Canonical Allele Identifier: CA2014120589

Gene: GAPDH

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534558T= , CM000674.2:g.6534558T=	GRCh38
NC_000012.11:g.6643724T= , CM000674.1:g.6643724T=	GRCh37
NC_000012.10:g.6513985T=	NCBI36
NG_007073.2:g.5068T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-35T= MANE Select	ENSP00000229239.5:n.-35T=
ENST00000229239.9:c.-35T=	ENSP00000229239.5:n.-35T=
ENST00000396856.5:c.-287T=	ENSP00000380065.1:n.-287T=
ENST00000396861.5:c.-127T=	ENSP00000380070.1:n.-127T=
ENST00000474249.5:n.18T=
ENST00000492719.5:n.26T=
ENST00000496049.1:n.47T=
NM_001289745.1:c.-127T=	NP_001276674.1:n.-127T=
NM_002046.5:c.-35T=	NP_002037.2:n.-35T=
NM_001289745.2:c.-127T=	NP_001276674.1:n.-127T=
NM_001357943.1:c.-35T=	NP_001344872.1:n.-35T=
NM_002046.6:c.-35T=	NP_002037.2:n.-35T=
NR_152150.1:n.42T=
NM_002046.7:c.-35T= MANE Select	NP_002037.2:n.-35T=
NM_001289745.3:c.-127T=	NP_001276674.1:n.-127T=
NM_001289746.2:c.-275T=	NP_001276675.1:n.-275T=
NM_001357943.2:c.-35T=	NP_001344872.1:n.-35T=
NR_152150.2:n.42T=