Canonical Allele Identifier: CA2014120661

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534656T= , CM000674.2:g.6534656T=	GRCh38
NC_000012.11:g.6643822T= , CM000674.1:g.6643822T=	GRCh37
NC_000012.10:g.6514083T=	NCBI36
NG_007073.2:g.5166T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+87T= MANE Select	ENSP00000229239.5:n.-24+87T=
ENST00000229239.9:c.-24+87T=	ENSP00000229239.5:n.-24+87T=
ENST00000396856.5:c.-276+87T=	ENSP00000380065.1:n.-276+87T=
ENST00000396861.5:c.-29T=	ENSP00000380070.1:n.-29T=
ENST00000474249.5:n.29+87T=
ENST00000492719.5:n.37+87T=
ENST00000496049.1:n.58+87T=
NM_001289745.1:c.-29T=	NP_001276674.1:n.-29T=
NM_002046.5:c.-24+87T=	NP_002037.2:n.-24+87T=
NM_001289745.2:c.-29T=	NP_001276674.1:n.-29T=
NM_001357943.1:c.-24+87T=	NP_001344872.1:n.-24+87T=
NM_002046.6:c.-24+87T=	NP_002037.2:n.-24+87T=
NR_152150.1:n.53+87T=
NM_002046.7:c.-24+87T= MANE Select	NP_002037.2:n.-24+87T=
NM_001289745.3:c.-29T=	NP_001276674.1:n.-29T=
NM_001289746.2:c.-177T=	NP_001276675.1:n.-177T=
NM_001357943.2:c.-24+87T=	NP_001344872.1:n.-24+87T=
NR_152150.2:n.53+87T=