Linked Data
ClinVar Variation Id:
1148963
ClinVar RCV Id:
RCV001489041
dbSNP Id:
rs2142987882
gnomAD v3:
17-7224373-T-C
gnomAD v4:
17-7224373-T-C
MyVariant Identifiers:
chr17:g.7127692T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.7224373T>C , CM000679.2:g.7224373T>C | GRCh38 |
| NC_000017.10:g.7127692T>C , CM000679.1:g.7127692T>C | GRCh37 |
| NC_000017.9:g.7068416T>C | NCBI36 |
| NG_007975.1:g.9540T>C | |
| NG_008391.2:g.678A>G | |
| NG_033038.1:g.15172A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000356839.10:c.1585T>C MANE Select | ENSP00000349297.5:p.Leu529= | |
| ENST00000322910.9:c.*1540T>C | ENSP00000325395.5:n.*1540T>C | |
| ENST00000350303.9:c.1519T>C | ENSP00000344152.5:p.Leu507= | |
| ENST00000356839.9:c.1585T>C | ENSP00000349297.5:p.Leu529= | |
| ENST00000542255.6:c.443T>C | ||
| ENST00000543245.6:c.1654T>C | ENSP00000438689.2:p.Leu552= | |
| ENST00000578319.5:n.80T>C | ||
| ENST00000578711.1:n.869T>C | ||
| ENST00000578809.5:n.157T>C | ||
| ENST00000579391.1:n.193T>C | ||
| ENST00000579425.5:n.701T>C | ||
| ENST00000579546.1:c.324T>C | ||
| ENST00000579894.5:n.372T>C | ||
| ENST00000582450.1:n.93T>C | ||
| ENST00000583074.5:n.206T>C | ||
| ENST00000583850.5:n.360T>C | ||
| ENST00000583858.5:c.516T>C | ||
| ENST00000585203.6:n.776T>C | ||
| NM_000018.3:c.1585T>C | NP_000009.1:p.Leu529= | |
| NM_001033859.2:c.1519T>C | NP_001029031.1:p.Leu507= | |
| NM_001270447.1:c.1654T>C | NP_001257376.1:p.Leu552= | |
| NM_001270448.1:c.1357T>C | NP_001257377.1:p.Leu453= | |
| XM_006721516.2:c.1585T>C | XP_006721579.2:p.Leu529= | |
| XM_011523829.1:c.1487T>C | XP_011522131.1:p.Val496Ala | |
| XM_011523830.1:c.1487T>C | XP_011522132.1:p.Val496Ala | |
| XR_934021.1:n.1692T>C | ||
| XR_934022.1:n.1594T>C | ||
| XR_934023.1:n.1594T>C | ||
| XM_006721516.3:c.1585T>C | XP_006721579.2:p.Leu529= | |
| XM_011523829.2:c.1487T>C | XP_011522131.1:p.Val496Ala | |
| XM_011523830.2:c.1487T>C | XP_011522132.1:p.Val496Ala | |
| XM_024450741.1:c.1487T>C | XP_024306509.1:p.Val496Ala | |
| XR_934021.2:n.1644T>C | ||
| XR_934022.2:n.1546T>C | ||
| XR_934023.2:n.1546T>C | ||
| NM_000018.4:c.1585T>C MANE Select | NP_000009.1:p.Leu529= | |
| NM_001033859.3:c.1519T>C | NP_001029031.1:p.Leu507= | |
| NM_001270447.2:c.1654T>C | NP_001257376.1:p.Leu552= | |
| NM_001270448.2:c.1357T>C | NP_001257377.1:p.Leu453= |