Canonical Allele Identifier: CA1266824908
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551870C= , CM000664.2:g.85551870C= GRCh38
NC_000002.11:g.85778993C= , CM000664.1:g.85778993C= GRCh37
NC_000002.10:g.85632504C= NCBI36
NG_011811.2:g.14665G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.6029G=
ENST00000482662.2:n.4436G=
ENST00000685865.1:n.2388G=
ENST00000687250.1:n.2088G=
ENST00000687995.1:n.1903G=
ENST00000688205.1:c.*1144G= ENSP00000509673.1:n.*1144G=
ENST00000688788.1:n.1790G=
ENST00000689276.1:c.1482G= ENSP00000510012.1:p.Gln494=
ENST00000689576.1:c.*170G= ENSP00000508712.1:n.*170G=
ENST00000690108.1:c.*1207G= ENSP00000510617.1:n.*1207G=
ENST00000690468.1:c.*103G= ENSP00000509078.1:n.*103G=
ENST00000690595.1:c.876G= ENSP00000508979.1:p.Gln292=
ENST00000691348.1:c.*103G= ENSP00000509369.1:n.*103G=
ENST00000691410.1:c.*1128G= ENSP00000508479.1:n.*1128G=
ENST00000693287.1:c.867G= ENSP00000510264.1:p.Gln289=
ENST00000693681.1:c.864G= ENSP00000510789.1:p.Gln288=
ENST00000233838.9:c.1551G= MANE Select ENSP00000233838.3:p.Gln517=
ENST00000233838.8:c.1551G= ENSP00000233838.3:p.Gln517=
ENST00000430215.7:c.1380G= ENSP00000408045.3:p.Gln460=
ENST00000465637.5:n.179-3866G=
NM_000821.5:c.1551G= NP_000812.2:p.Gln517=
NM_000821.6:c.1551G= NP_000812.2:p.Gln517=
NM_001142269.2:c.1380G= NP_001135741.1:p.Gln460=
NM_001142269.3:c.1380G= NP_001135741.1:p.Gln460=
XM_005264259.3:c.1551G= XP_005264316.1:p.Gln517=
XM_011532764.1:c.729G= XP_011531066.1:p.Gln243=
XM_011532765.1:c.729G= XP_011531067.1:p.Gln243=
XR_939677.1:n.1464G=
XM_005264259.5:c.1551G= XP_005264316.1:p.Gln517=
XM_011532764.3:c.729G= XP_011531066.1:p.Gln243=
XM_011532765.3:c.729G= XP_011531067.1:p.Gln243=
XM_017003803.2:c.1380G= XP_016859292.1:p.Gln460=
XR_001738703.2:n.1464G=
NM_000821.7:c.1551G= MANE Select NP_000812.2:p.Gln517=
NM_001142269.4:c.1380G= NP_001135741.1:p.Gln460=