HGVS | Genome Assembly |
---|---|
NC_000017.11:g.7223827G>A , CM000679.2:g.7223827G>A | GRCh38 |
NC_000017.10:g.7127146G>A , CM000679.1:g.7127146G>A | GRCh37 |
NC_000017.9:g.7067870G>A | NCBI36 |
NG_007975.1:g.8994G>A | |
NG_008391.2:g.1224C>T | |
NG_033038.1:g.15718C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000356839.10:c.1284G>A MANE Select | ENSP00000349297.5:p.Lys428= | |
ENST00000322910.9:c.*1239G>A | ENSP00000325395.5:n.*1239G>A | |
ENST00000350303.9:c.1218G>A | ENSP00000344152.5:p.Lys406= | |
ENST00000356839.9:c.1284G>A | ENSP00000349297.5:p.Lys428= | |
ENST00000542255.6:c.142G>A | ||
ENST00000543245.6:c.1353G>A | ENSP00000438689.2:p.Lys451= | |
ENST00000578579.2:n.455G>A | ||
ENST00000578711.1:n.323G>A | ||
ENST00000578824.5:n.700G>A | ||
ENST00000579425.5:n.308G>A | ||
ENST00000579546.1:c.121G>A | ||
ENST00000583074.5:n.3G>A | ||
ENST00000583850.5:n.59G>A | ||
ENST00000583858.5:c.313G>A | ||
ENST00000585203.6:n.492G>A | ||
NM_000018.3:c.1284G>A | NP_000009.1:p.Lys428= | |
NM_001033859.2:c.1218G>A | NP_001029031.1:p.Lys406= | |
NM_001270447.1:c.1353G>A | NP_001257376.1:p.Lys451= | |
NM_001270448.1:c.1056G>A | NP_001257377.1:p.Lys352= | |
XM_006721516.2:c.1284G>A | XP_006721579.2:p.Lys428= | |
XM_011523829.1:c.1284G>A | XP_011522131.1:p.Lys428= | |
XM_011523830.1:c.1284G>A | XP_011522132.1:p.Lys428= | |
XR_934021.1:n.1391G>A | ||
XR_934022.1:n.1391G>A | ||
XR_934023.1:n.1391G>A | ||
XM_006721516.3:c.1284G>A | XP_006721579.2:p.Lys428= | |
XM_011523829.2:c.1284G>A | XP_011522131.1:p.Lys428= | |
XM_011523830.2:c.1284G>A | XP_011522132.1:p.Lys428= | |
XM_024450741.1:c.1284G>A | XP_024306509.1:p.Lys428= | |
XR_934021.2:n.1343G>A | ||
XR_934022.2:n.1343G>A | ||
XR_934023.2:n.1343G>A | ||
NM_000018.4:c.1284G>A MANE Select | NP_000009.1:p.Lys428= | |
NM_001033859.3:c.1218G>A | NP_001029031.1:p.Lys406= | |
NM_001270447.2:c.1353G>A | NP_001257376.1:p.Lys451= | |
NM_001270448.2:c.1056G>A | NP_001257377.1:p.Lys352= |