Canonical Allele Identifier: CA1266820878

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85546474T= , CM000664.2:g.85546474T=	GRCh38
NC_000002.11:g.85773597T= , CM000664.1:g.85773597T=	GRCh37
NC_000002.10:g.85627108T=	NCBI36
NG_011811.2:g.20061A=
NG_029183.1:g.12497T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233838.9:c.*3460A= MANE Select	ENSP00000233838.3:n.*3460A=
ENST00000233838.8:c.*3460A=	ENSP00000233838.3:n.*3460A=
NM_000821.5:c.*3460A=	NP_000812.2:n.*3460A=
NM_000821.6:c.*3460A=	NP_000812.2:n.*3460A=
NM_001142269.2:c.*3460A=	NP_001135741.1:n.*3460A=
NM_001142269.3:c.*3460A=	NP_001135741.1:n.*3460A=
NM_000821.7:c.*3460A= MANE Select	NP_000812.2:n.*3460A=
NM_001142269.4:c.*3460A=	NP_001135741.1:n.*3460A=