Canonical Allele Identifier: CA1266825412
Gene: GGCX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.85553045A= , CM000664.2:g.85553045A= GRCh38
NC_000002.11:g.85780168A= , CM000664.1:g.85780168A= GRCh37
NC_000002.10:g.85633679A= NCBI36
NG_011811.2:g.13490T=

Transcript Alleles

HGVS Amino-acid Change
NM_000821.7:c.1181T= MANE Select NP_000812.2:p.Leu394=
ENST00000233838.9:c.1181T= MANE Select ENSP00000233838.3:p.Leu394=
NM_000821.5:c.1181T= NP_000812.2:p.Leu394=
NM_000821.6:c.1181T= NP_000812.2:p.Leu394=
NM_001142269.2:c.1010T= NP_001135741.1:p.Leu337=
NM_001142269.3:c.1010T= NP_001135741.1:p.Leu337=
NM_001142269.4:c.1010T= NP_001135741.1:p.Leu337=
ENST00000233838.8:c.1181T= ENSP00000233838.3:p.Leu394=
ENST00000430215.7:c.1010T= ENSP00000408045.3:p.Leu337=
ENST00000465637.5:n.179-5041T=
ENST00000473665.1:n.674T=
ENST00000473665.2:n.5225T=
ENST00000482662.1:n.598T=
ENST00000482662.2:n.3632T=
ENST00000685865.1:n.1584T=
ENST00000687250.1:n.1284T=
ENST00000687995.1:n.1533T=
ENST00000688205.1:c.*774T= ENSP00000509673.1:n.*774T=
ENST00000688788.1:n.1420T=
ENST00000689276.1:c.1112T= ENSP00000510012.1:p.Leu371=
ENST00000689576.1:c.1181T= ENSP00000508712.1:p.Leu394=
ENST00000690108.1:c.*837T= ENSP00000510617.1:n.*837T=
ENST00000690468.1:c.902T= ENSP00000509078.1:p.Leu301=
ENST00000690595.1:c.506T= ENSP00000508979.1:p.Leu169=
ENST00000691348.1:c.1010T= ENSP00000509369.1:p.Leu337=
ENST00000691410.1:c.*758T= ENSP00000508479.1:n.*758T=
ENST00000693287.1:c.497T= ENSP00000510264.1:p.Leu166=
ENST00000693681.1:c.494T= ENSP00000510789.1:p.Leu165=
XM_005264259.3:c.1181T= XP_005264316.1:p.Leu394=
XM_005264259.5:c.1181T= XP_005264316.1:p.Leu394=
XM_011532764.1:c.359T= XP_011531066.1:p.Leu120=
XM_011532764.3:c.359T= XP_011531066.1:p.Leu120=
XM_011532765.1:c.359T= XP_011531067.1:p.Leu120=
XM_011532765.3:c.359T= XP_011531067.1:p.Leu120=
XM_017003803.2:c.1010T= XP_016859292.1:p.Leu337=
XR_001738703.2:n.1246T=
XR_939677.1:n.1246T=