Canonical Allele Identifier: CA2014120838

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534843T= , CM000674.2:g.6534843T=	GRCh38
NC_000012.11:g.6644009T= , CM000674.1:g.6644009T=	GRCh37
NC_000012.10:g.6514270T=	NCBI36
NG_007073.2:g.5353T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.11T= MANE Select	ENSP00000229239.5:p.Val4=
ENST00000229239.9:c.11T=	ENSP00000229239.5:p.Val4=
ENST00000396856.5:c.-242T=	ENSP00000380065.1:n.-242T=
ENST00000396859.5:c.11T=	ENSP00000380068.1:p.Val4=
ENST00000396861.5:c.11T=	ENSP00000380070.1:p.Val4=
ENST00000466525.1:n.52T=
ENST00000466588.5:n.90T=
ENST00000474249.5:n.63T=
ENST00000492719.5:n.71T=
ENST00000496049.1:n.92T=
NM_001289745.1:c.11T=	NP_001276674.1:p.Val4=
NM_001289746.1:c.11T=	NP_001276675.1:p.Val4=
NM_002046.5:c.11T=	NP_002037.2:p.Val4=
NM_001289745.2:c.11T=	NP_001276674.1:p.Val4=
NM_001357943.1:c.11T=	NP_001344872.1:p.Val4=
NM_002046.6:c.11T=	NP_002037.2:p.Val4=
NR_152150.1:n.87T=
NM_002046.7:c.11T= MANE Select	NP_002037.2:p.Val4=
NM_001289745.3:c.11T=	NP_001276674.1:p.Val4=
NM_001289746.2:c.11T=	NP_001276675.1:p.Val4=
NM_001357943.2:c.11T=	NP_001344872.1:p.Val4=
NR_152150.2:n.87T=