Canonical Allele Identifier: CA1266825498

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85553233T= , CM000664.2:g.85553233T=	GRCh38
NC_000002.11:g.85780356T= , CM000664.1:g.85780356T=	GRCh37
NC_000002.10:g.85633867T=	NCBI36
NG_011811.2:g.13302A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000473665.2:n.5198A=
ENST00000482662.2:n.3605A=
ENST00000685865.1:n.1557A=
ENST00000687250.1:n.1257A=
ENST00000687995.1:n.1506A=
ENST00000688205.1:c.*747A=	ENSP00000509673.1:n.*747A=
ENST00000688788.1:n.1393A=
ENST00000689276.1:c.1085A=	ENSP00000510012.1:p.Gln362=
ENST00000689576.1:c.1154A=	ENSP00000508712.1:p.Gln385=
ENST00000690108.1:c.*810A=	ENSP00000510617.1:n.*810A=
ENST00000690468.1:c.875A=	ENSP00000509078.1:p.Gln292=
ENST00000690595.1:c.479A=	ENSP00000508979.1:p.Gln160=
ENST00000691348.1:c.983A=	ENSP00000509369.1:p.Gln328=
ENST00000691410.1:c.*731A=	ENSP00000508479.1:n.*731A=
ENST00000693287.1:c.470A=	ENSP00000510264.1:p.Gln157=
ENST00000693681.1:c.467A=	ENSP00000510789.1:p.Gln156=
ENST00000233838.9:c.1154A= MANE Select	ENSP00000233838.3:p.Gln385=
ENST00000233838.8:c.1154A=	ENSP00000233838.3:p.Gln385=
ENST00000430215.7:c.983A=	ENSP00000408045.3:p.Gln328=
ENST00000465637.5:n.179-5229A=
ENST00000473665.1:n.647A=
ENST00000482662.1:n.571A=
NM_000821.5:c.1154A=	NP_000812.2:p.Gln385=
NM_000821.6:c.1154A=	NP_000812.2:p.Gln385=
NM_001142269.2:c.983A=	NP_001135741.1:p.Gln328=
NM_001142269.3:c.983A=	NP_001135741.1:p.Gln328=
XM_005264259.3:c.1154A=	XP_005264316.1:p.Gln385=
XM_011532764.1:c.332A=	XP_011531066.1:p.Gln111=
XM_011532765.1:c.332A=	XP_011531067.1:p.Gln111=
XR_939677.1:n.1219A=
XM_005264259.5:c.1154A=	XP_005264316.1:p.Gln385=
XM_011532764.3:c.332A=	XP_011531066.1:p.Gln111=
XM_011532765.3:c.332A=	XP_011531067.1:p.Gln111=
XM_017003803.2:c.983A=	XP_016859292.1:p.Gln328=
XR_001738703.2:n.1219A=
NM_000821.7:c.1154A= MANE Select	NP_000812.2:p.Gln385=
NM_001142269.4:c.983A=	NP_001135741.1:p.Gln328=