Canonical Allele Identifier: CA2014120844

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534852G= , CM000674.2:g.6534852G=	GRCh38
NC_000012.11:g.6644018G= , CM000674.1:g.6644018G=	GRCh37
NC_000012.10:g.6514279G=	NCBI36
NG_007073.2:g.5362G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.20G= MANE Select	ENSP00000229239.5:p.Gly7=
ENST00000229239.9:c.20G=	ENSP00000229239.5:p.Gly7=
ENST00000396856.5:c.-233G=	ENSP00000380065.1:n.-233G=
ENST00000396859.5:c.20G=	ENSP00000380068.1:p.Gly7=
ENST00000396861.5:c.20G=	ENSP00000380070.1:p.Gly7=
ENST00000466525.1:n.61G=
ENST00000466588.5:n.99G=
ENST00000474249.5:n.72G=
ENST00000492719.5:n.80G=
ENST00000496049.1:n.101G=
NM_001289745.1:c.20G=	NP_001276674.1:p.Gly7=
NM_001289746.1:c.20G=	NP_001276675.1:p.Gly7=
NM_002046.5:c.20G=	NP_002037.2:p.Gly7=
NM_001289745.2:c.20G=	NP_001276674.1:p.Gly7=
NM_001357943.1:c.20G=	NP_001344872.1:p.Gly7=
NM_002046.6:c.20G=	NP_002037.2:p.Gly7=
NR_152150.1:n.96G=
NM_002046.7:c.20G= MANE Select	NP_002037.2:p.Gly7=
NM_001289745.3:c.20G=	NP_001276674.1:p.Gly7=
NM_001289746.2:c.20G=	NP_001276675.1:p.Gly7=
NM_001357943.2:c.20G=	NP_001344872.1:p.Gly7=
NR_152150.2:n.96G=