Canonical Allele Identifier: CA2014120640

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534634A= , CM000674.2:g.6534634A=	GRCh38
NC_000012.11:g.6643800A= , CM000674.1:g.6643800A=	GRCh37
NC_000012.10:g.6514061A=	NCBI36
NG_007073.2:g.5144A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+65A= MANE Select	ENSP00000229239.5:n.-24+65A=
ENST00000229239.9:c.-24+65A=	ENSP00000229239.5:n.-24+65A=
ENST00000396856.5:c.-276+65A=	ENSP00000380065.1:n.-276+65A=
ENST00000396861.5:c.-51A=	ENSP00000380070.1:n.-51A=
ENST00000474249.5:n.29+65A=
ENST00000492719.5:n.37+65A=
ENST00000496049.1:n.58+65A=
NM_001289745.1:c.-51A=	NP_001276674.1:n.-51A=
NM_002046.5:c.-24+65A=	NP_002037.2:n.-24+65A=
NM_001289745.2:c.-51A=	NP_001276674.1:n.-51A=
NM_001357943.1:c.-24+65A=	NP_001344872.1:n.-24+65A=
NM_002046.6:c.-24+65A=	NP_002037.2:n.-24+65A=
NR_152150.1:n.53+65A=
NM_002046.7:c.-24+65A= MANE Select	NP_002037.2:n.-24+65A=
NM_001289745.3:c.-51A=	NP_001276674.1:n.-51A=
NM_001289746.2:c.-199A=	NP_001276675.1:n.-199A=
NM_001357943.2:c.-24+65A=	NP_001344872.1:n.-24+65A=
NR_152150.2:n.53+65A=