Canonical Allele Identifier: CA2014120641

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534635G= , CM000674.2:g.6534635G=	GRCh38
NC_000012.11:g.6643801G= , CM000674.1:g.6643801G=	GRCh37
NC_000012.10:g.6514062G=	NCBI36
NG_007073.2:g.5145G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+66G= MANE Select	ENSP00000229239.5:n.-24+66G=
ENST00000229239.9:c.-24+66G=	ENSP00000229239.5:n.-24+66G=
ENST00000396856.5:c.-276+66G=	ENSP00000380065.1:n.-276+66G=
ENST00000396861.5:c.-50G=	ENSP00000380070.1:n.-50G=
ENST00000474249.5:n.29+66G=
ENST00000492719.5:n.37+66G=
ENST00000496049.1:n.58+66G=
NM_001289745.1:c.-50G=	NP_001276674.1:n.-50G=
NM_002046.5:c.-24+66G=	NP_002037.2:n.-24+66G=
NM_001289745.2:c.-50G=	NP_001276674.1:n.-50G=
NM_001357943.1:c.-24+66G=	NP_001344872.1:n.-24+66G=
NM_002046.6:c.-24+66G=	NP_002037.2:n.-24+66G=
NR_152150.1:n.53+66G=
NM_002046.7:c.-24+66G= MANE Select	NP_002037.2:n.-24+66G=
NM_001289745.3:c.-50G=	NP_001276674.1:n.-50G=
NM_001289746.2:c.-198G=	NP_001276675.1:n.-198G=
NM_001357943.2:c.-24+66G=	NP_001344872.1:n.-24+66G=
NR_152150.2:n.53+66G=