Canonical Allele Identifier: CA2617278818

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534754-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534754A>C , CM000674.2:g.6534754A>C	GRCh38
NC_000012.11:g.6643920A>C , CM000674.1:g.6643920A>C	GRCh37
NC_000012.10:g.6514181A>C	NCBI36
NG_007073.2:g.5264A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-23-56A>C MANE Select	ENSP00000229239.5:n.-23-56A>C
ENST00000229239.9:c.-23-56A>C	ENSP00000229239.5:n.-23-56A>C
ENST00000396856.5:c.-275-56A>C	ENSP00000380065.1:n.-275-56A>C
ENST00000396859.5:c.-79A>C	ENSP00000380068.1:n.-79A>C
ENST00000396861.5:c.-23-56A>C	ENSP00000380070.1:n.-23-56A>C
ENST00000466588.5:n.1A>C
ENST00000474249.5:n.30-56A>C
ENST00000492719.5:n.38-56A>C
ENST00000496049.1:n.59-56A>C
NM_001289745.1:c.-23-56A>C	NP_001276674.1:n.-23-56A>C
NM_001289746.1:c.-79A>C	NP_001276675.1:n.-79A>C
NM_002046.5:c.-23-56A>C	NP_002037.2:n.-23-56A>C
NM_001289745.2:c.-23-56A>C	NP_001276674.1:n.-23-56A>C
NM_001357943.1:c.-23-56A>C	NP_001344872.1:n.-23-56A>C
NM_002046.6:c.-23-56A>C	NP_002037.2:n.-23-56A>C
NR_152150.1:n.54-56A>C
NM_002046.7:c.-23-56A>C MANE Select	NP_002037.2:n.-23-56A>C
NM_001289745.3:c.-23-56A>C	NP_001276674.1:n.-23-56A>C
NM_001289746.2:c.-79A>C	NP_001276675.1:n.-79A>C
NM_001357943.2:c.-23-56A>C	NP_001344872.1:n.-23-56A>C
NR_152150.2:n.54-56A>C