Canonical Allele Identifier: CA2014120541

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534523T= , CM000674.2:g.6534523T=	GRCh38
NC_000012.11:g.6643689T= , CM000674.1:g.6643689T=	GRCh37
NC_000012.10:g.6513950T=	NCBI36
NG_007073.2:g.5033T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-70T= MANE Select	ENSP00000229239.5:n.-70T=
ENST00000229239.9:c.-70T=	ENSP00000229239.5:n.-70T=
ENST00000496049.1:n.12T=
NM_001289745.1:c.-162T=	NP_001276674.1:n.-162T=
NM_002046.5:c.-70T=	NP_002037.2:n.-70T=
NM_001289745.2:c.-162T=	NP_001276674.1:n.-162T=
NM_001357943.1:c.-70T=	NP_001344872.1:n.-70T=
NM_002046.6:c.-70T=	NP_002037.2:n.-70T=
NR_152150.1:n.7T=
NM_002046.7:c.-70T= MANE Select	NP_002037.2:n.-70T=
NM_001289745.3:c.-162T=	NP_001276674.1:n.-162T=
NM_001289746.2:c.-310T=	NP_001276675.1:n.-310T=
NM_001357943.2:c.-70T=	NP_001344872.1:n.-70T=
NR_152150.2:n.7T=