HGVS | Genome Assembly |
---|---|
NC_000013.11:g.20189067_20189068delinsCA , CM000675.2:g.20189067_20189068delinsCA | GRCh38 |
NC_000013.10:g.20763206_20763207delinsCA , CM000675.1:g.20763206_20763207delinsCA | GRCh37 |
NC_000013.9:g.19661206_19661207delinsCA | NCBI36 |
NG_008358.1:g.8908_8909delinsTG |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000382844.2:c.514_515delinsTG | ENSP00000372295.1:p.Trp172= | |
ENST00000382848.5:c.514_515delinsTG MANE Select | ENSP00000372299.4:p.Trp172= | |
ENST00000382844.1:c.514_515delinsTG | ENSP00000372295.1:p.Trp172= | |
ENST00000382848.4:c.514_515delinsTG | ENSP00000372299.4:p.Trp172= | |
NM_004004.5:c.514_515delinsTG | NP_003995.2:p.Trp172= | |
XM_011535049.1:c.514_515delinsTG | XP_011533351.1:p.Trp172= | |
XM_011535049.2:c.514_515delinsTG | XP_011533351.1:p.Trp172= | |
NM_004004.6:c.514_515delinsTG MANE Select | NP_003995.2:p.Trp172= |