Canonical Allele Identifier: CA2014120645

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534638C= , CM000674.2:g.6534638C=	GRCh38
NC_000012.11:g.6643804C= , CM000674.1:g.6643804C=	GRCh37
NC_000012.10:g.6514065C=	NCBI36
NG_007073.2:g.5148C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+69C= MANE Select	ENSP00000229239.5:n.-24+69C=
ENST00000229239.9:c.-24+69C=	ENSP00000229239.5:n.-24+69C=
ENST00000396856.5:c.-276+69C=	ENSP00000380065.1:n.-276+69C=
ENST00000396861.5:c.-47C=	ENSP00000380070.1:n.-47C=
ENST00000474249.5:n.29+69C=
ENST00000492719.5:n.37+69C=
ENST00000496049.1:n.58+69C=
NM_001289745.1:c.-47C=	NP_001276674.1:n.-47C=
NM_002046.5:c.-24+69C=	NP_002037.2:n.-24+69C=
NM_001289745.2:c.-47C=	NP_001276674.1:n.-47C=
NM_001357943.1:c.-24+69C=	NP_001344872.1:n.-24+69C=
NM_002046.6:c.-24+69C=	NP_002037.2:n.-24+69C=
NR_152150.1:n.53+69C=
NM_002046.7:c.-24+69C= MANE Select	NP_002037.2:n.-24+69C=
NM_001289745.3:c.-47C=	NP_001276674.1:n.-47C=
NM_001289746.2:c.-195C=	NP_001276675.1:n.-195C=
NM_001357943.2:c.-24+69C=	NP_001344872.1:n.-24+69C=
NR_152150.2:n.53+69C=