MyVariant.info:
GRCh37
chr5:g.112178329A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.112842632A>G , CM000667.2:g.112842632A>G | GRCh38 |
| NC_000005.9:g.112178329A>G , CM000667.1:g.112178329A>G | GRCh37 |
| NC_000005.8:g.112206228A>G | NCBI36 |
| NG_008481.4:g.155112A>G , LRG_130:g.155112A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000504915.3:c.7092A>G | ENSP00000473355.2:p.Pro2364= | |
| ENST00000505350.2:c.*7044A>G | ENSP00000481752.1:n.*7044A>G | |
| ENST00000507379.6:c.6984A>G | ENSP00000423224.2:p.Pro2328= | |
| ENST00000509732.6:c.7038A>G | ENSP00000426541.2:p.Pro2346= | |
| ENST00000512211.7:c.7038A>G | ENSP00000423828.3:p.Pro2346= | |
| ENST00000257430.9:c.7038A>G MANE Select | ENSP00000257430.4:p.Pro2346= | |
| ENST00000257430.8:c.7038A>G | ENSP00000257430.4:p.Pro2346= | |
| ENST00000508376.6:c.7038A>G | ENSP00000427089.2:p.Pro2346= | |
| ENST00000508624.5:c.*6360A>G | ENSP00000424265.1:n.*6360A>G | |
| ENST00000520401.1:c.230+13660A>G | ||
| NM_000038.5:c.7038A>G | NP_000029.2:p.Pro2346= | |
| NM_001127510.2:c.7038A>G | NP_001120982.1:p.Pro2346= | |
| NM_001127511.2:c.6984A>G | NP_001120983.2:p.Pro2328= | |
| NM_001354895.1:c.7038A>G | NP_001341824.1:p.Pro2346= | |
| NM_001354896.1:c.7092A>G | NP_001341825.1:p.Pro2364= | |
| NM_001354897.1:c.7068A>G | NP_001341826.1:p.Pro2356= | |
| NM_001354898.1:c.6963A>G | NP_001341827.1:p.Pro2321= | |
| NM_001354899.1:c.6954A>G | NP_001341828.1:p.Pro2318= | |
| NM_001354900.1:c.6915A>G | NP_001341829.1:p.Pro2305= | |
| NM_001354901.1:c.6861A>G | NP_001341830.1:p.Pro2287= | |
| NM_001354902.1:c.6765A>G | NP_001341831.1:p.Pro2255= | |
| NM_001354903.1:c.6735A>G | NP_001341832.1:p.Pro2245= | |
| NM_001354904.1:c.6660A>G | NP_001341833.1:p.Pro2220= | |
| NM_001354905.1:c.6558A>G | NP_001341834.1:p.Pro2186= | |
| NM_001354906.1:c.6189A>G | NP_001341835.1:p.Pro2063= | |
| NM_000038.6:c.7038A>G MANE Select | NP_000029.2:p.Pro2346= | |
| NM_001127510.3:c.7038A>G | NP_001120982.1:p.Pro2346= | |
| NM_001127511.3:c.6984A>G | NP_001120983.2:p.Pro2328= | |
| NM_001354895.2:c.7038A>G | NP_001341824.1:p.Pro2346= | |
| NM_001354896.2:c.7092A>G | NP_001341825.1:p.Pro2364= | |
| NM_001354897.2:c.7068A>G | NP_001341826.1:p.Pro2356= | |
| NM_001354898.2:c.6963A>G | NP_001341827.1:p.Pro2321= | |
| NM_001354899.2:c.6954A>G | NP_001341828.1:p.Pro2318= | |
| NM_001354900.2:c.6915A>G | NP_001341829.1:p.Pro2305= | |
| NM_001354901.2:c.6861A>G | NP_001341830.1:p.Pro2287= | |
| NM_001354902.2:c.6765A>G | NP_001341831.1:p.Pro2255= | |
| NM_001354903.2:c.6735A>G | NP_001341832.1:p.Pro2245= | |
| NM_001354904.2:c.6660A>G | NP_001341833.1:p.Pro2220= | |
| NM_001354905.2:c.6558A>G | NP_001341834.1:p.Pro2186= | |
| NM_001354906.2:c.6189A>G | NP_001341835.1:p.Pro2063= |