Canonical Allele Identifier: CA2014120845

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534853A= , CM000674.2:g.6534853A=	GRCh38
NC_000012.11:g.6644019A= , CM000674.1:g.6644019A=	GRCh37
NC_000012.10:g.6514280A=	NCBI36
NG_007073.2:g.5363A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.21A= MANE Select	ENSP00000229239.5:p.Gly7=
ENST00000229239.9:c.21A=	ENSP00000229239.5:p.Gly7=
ENST00000396856.5:c.-232A=	ENSP00000380065.1:n.-232A=
ENST00000396859.5:c.21A=	ENSP00000380068.1:p.Gly7=
ENST00000396861.5:c.21A=	ENSP00000380070.1:p.Gly7=
ENST00000466525.1:n.62A=
ENST00000466588.5:n.100A=
ENST00000474249.5:n.73A=
ENST00000492719.5:n.81A=
ENST00000496049.1:n.102A=
NM_001289745.1:c.21A=	NP_001276674.1:p.Gly7=
NM_001289746.1:c.21A=	NP_001276675.1:p.Gly7=
NM_002046.5:c.21A=	NP_002037.2:p.Gly7=
NM_001289745.2:c.21A=	NP_001276674.1:p.Gly7=
NM_001357943.1:c.21A=	NP_001344872.1:p.Gly7=
NM_002046.6:c.21A=	NP_002037.2:p.Gly7=
NR_152150.1:n.97A=
NM_002046.7:c.21A= MANE Select	NP_002037.2:p.Gly7=
NM_001289745.3:c.21A=	NP_001276674.1:p.Gly7=
NM_001289746.2:c.21A=	NP_001276675.1:p.Gly7=
NM_001357943.2:c.21A=	NP_001344872.1:p.Gly7=
NR_152150.2:n.97A=