Canonical Allele Identifier: CA2014120649

Gene: GAPDH

Linked Data

• dbSNP Id: rs1592182764

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534641A>T , CM000674.2:g.6534641A>T	GRCh38
NC_000012.11:g.6643807A>T , CM000674.1:g.6643807A>T	GRCh37
NC_000012.10:g.6514068A>T	NCBI36
NG_007073.2:g.5151A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+72A>T MANE Select	ENSP00000229239.5:n.-24+72A>T
ENST00000229239.9:c.-24+72A>T	ENSP00000229239.5:n.-24+72A>T
ENST00000396856.5:c.-276+72A>T	ENSP00000380065.1:n.-276+72A>T
ENST00000396861.5:c.-44A>T	ENSP00000380070.1:n.-44A>T
ENST00000474249.5:n.29+72A>T
ENST00000492719.5:n.37+72A>T
ENST00000496049.1:n.58+72A>T
NM_001289745.1:c.-44A>T	NP_001276674.1:n.-44A>T
NM_002046.5:c.-24+72A>T	NP_002037.2:n.-24+72A>T
NM_001289745.2:c.-44A>T	NP_001276674.1:n.-44A>T
NM_001357943.1:c.-24+72A>T	NP_001344872.1:n.-24+72A>T
NM_002046.6:c.-24+72A>T	NP_002037.2:n.-24+72A>T
NR_152150.1:n.53+72A>T
NM_002046.7:c.-24+72A>T MANE Select	NP_002037.2:n.-24+72A>T
NM_001289745.3:c.-44A>T	NP_001276674.1:n.-44A>T
NM_001289746.2:c.-192A>T	NP_001276675.1:n.-192A>T
NM_001357943.2:c.-24+72A>T	NP_001344872.1:n.-24+72A>T
NR_152150.2:n.53+72A>T