Canonical Allele Identifier: CA1266819932

Gene: GGCX

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.85545889T= , CM000664.2:g.85545889T=	GRCh38
NC_000002.11:g.85773012T= , CM000664.1:g.85773012T=	GRCh37
NC_000002.10:g.85626523T=	NCBI36
NG_011811.2:g.20646A=
NG_029183.1:g.11912T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000233838.9:c.*4045A= MANE Select	ENSP00000233838.3:n.*4045A=
ENST00000233838.8:c.*4045A=	ENSP00000233838.3:n.*4045A=
NM_000821.5:c.*4045A=	NP_000812.2:n.*4045A=
NM_000821.6:c.*4045A=	NP_000812.2:n.*4045A=
NM_001142269.2:c.*4045A=	NP_001135741.1:n.*4045A=
NM_001142269.3:c.*4045A=	NP_001135741.1:n.*4045A=
NM_000821.7:c.*4045A= MANE Select	NP_000812.2:n.*4045A=
NM_001142269.4:c.*4045A=	NP_001135741.1:n.*4045A=