Canonical Allele Identifier: CA1266824938
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85551945A= , CM000664.2:g.85551945A= GRCh38
NC_000002.11:g.85779068A= , CM000664.1:g.85779068A= GRCh37
NC_000002.10:g.85632579A= NCBI36
NG_011811.2:g.14590T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000473665.2:n.5954T=
ENST00000482662.2:n.4361T=
ENST00000685865.1:n.2313T=
ENST00000687250.1:n.2013T=
ENST00000687995.1:n.1828T=
ENST00000688205.1:c.*1069T= ENSP00000509673.1:n.*1069T=
ENST00000688788.1:n.1715T=
ENST00000689276.1:c.1407T= ENSP00000510012.1:p.Ala469=
ENST00000689576.1:c.*95T= ENSP00000508712.1:n.*95T=
ENST00000690108.1:c.*1132T= ENSP00000510617.1:n.*1132T=
ENST00000690468.1:c.*28T= ENSP00000509078.1:n.*28T=
ENST00000690595.1:c.801T= ENSP00000508979.1:p.Ala267=
ENST00000691348.1:c.*28T= ENSP00000509369.1:n.*28T=
ENST00000691410.1:c.*1053T= ENSP00000508479.1:n.*1053T=
ENST00000693287.1:c.792T= ENSP00000510264.1:p.Ala264=
ENST00000693681.1:c.789T= ENSP00000510789.1:p.Ala263=
ENST00000233838.9:c.1476T= MANE Select ENSP00000233838.3:p.Ala492=
ENST00000233838.8:c.1476T= ENSP00000233838.3:p.Ala492=
ENST00000430215.7:c.1305T= ENSP00000408045.3:p.Ala435=
ENST00000465637.5:n.179-3941T=
NM_000821.5:c.1476T= NP_000812.2:p.Ala492=
NM_000821.6:c.1476T= NP_000812.2:p.Ala492=
NM_001142269.2:c.1305T= NP_001135741.1:p.Ala435=
NM_001142269.3:c.1305T= NP_001135741.1:p.Ala435=
XM_005264259.3:c.1476T= XP_005264316.1:p.Ala492=
XM_011532764.1:c.654T= XP_011531066.1:p.Ala218=
XM_011532765.1:c.654T= XP_011531067.1:p.Ala218=
XR_939677.1:n.1389T=
XM_005264259.5:c.1476T= XP_005264316.1:p.Ala492=
XM_011532764.3:c.654T= XP_011531066.1:p.Ala218=
XM_011532765.3:c.654T= XP_011531067.1:p.Ala218=
XM_017003803.2:c.1305T= XP_016859292.1:p.Ala435=
XR_001738703.2:n.1389T=
NM_000821.7:c.1476T= MANE Select NP_000812.2:p.Ala492=
NM_001142269.4:c.1305T= NP_001135741.1:p.Ala435=