Canonical Allele Identifier: CA2014122062

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6536732G= , CM000674.2:g.6536732G=	GRCh38
NC_000012.11:g.6645898G= , CM000674.1:g.6645898G=	GRCh37
NC_000012.10:g.6516159G=	NCBI36
NG_007073.2:g.7242G=

Transcript Alleles

HGVS	Amino-acid Change
NM_002046.7:c.178G= MANE Select	NP_002037.2:p.Val60=
ENST00000229239.10:c.178G= MANE Select	ENSP00000229239.5:p.Val60=
NM_001256799.2:c.52G=	NP_001243728.1:p.Val18=
NM_001256799.3:c.52G=	NP_001243728.1:p.Val18=
NM_001289745.1:c.178G=	NP_001276674.1:p.Val60=
NM_001289745.2:c.178G=	NP_001276674.1:p.Val60=
NM_001289745.3:c.178G=	NP_001276674.1:p.Val60=
NM_001289746.1:c.178G=	NP_001276675.1:p.Val60=
NM_001289746.2:c.178G=	NP_001276675.1:p.Val60=
NM_001357943.1:c.130-6G=	NP_001344872.1:n.130-6G=
NM_001357943.2:c.130-6G=	NP_001344872.1:n.130-6G=
NM_002046.5:c.178G=	NP_002037.2:p.Val60=
NM_002046.6:c.178G=	NP_002037.2:p.Val60=
NR_152150.1:n.254G=
NR_152150.2:n.254G=
ENST00000229239.9:c.178G=	ENSP00000229239.5:p.Val60=
ENST00000396856.5:c.-75G=	ENSP00000380065.1:n.-75G=
ENST00000396858.5:c.52G=	ENSP00000380067.1:p.Val18=
ENST00000396859.5:c.178G=	ENSP00000380068.1:p.Val60=
ENST00000396861.5:c.178G=	ENSP00000380070.1:p.Val60=
ENST00000466525.1:n.219G=
ENST00000466588.5:n.257G=
ENST00000474249.5:n.230G=
ENST00000492719.5:n.368G=
ENST00000619601.1:c.52G=	ENSP00000478864.1:p.Val18=