Canonical Allele Identifier: CA2617278521

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534590-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534590A>C , CM000674.2:g.6534590A>C	GRCh38
NC_000012.11:g.6643756A>C , CM000674.1:g.6643756A>C	GRCh37
NC_000012.10:g.6514017A>C	NCBI36
NG_007073.2:g.5100A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+21A>C MANE Select	ENSP00000229239.5:n.-24+21A>C
ENST00000229239.9:c.-24+21A>C	ENSP00000229239.5:n.-24+21A>C
ENST00000396856.5:c.-276+21A>C	ENSP00000380065.1:n.-276+21A>C
ENST00000396861.5:c.-95A>C	ENSP00000380070.1:n.-95A>C
ENST00000474249.5:n.29+21A>C
ENST00000492719.5:n.37+21A>C
ENST00000496049.1:n.58+21A>C
NM_001289745.1:c.-95A>C	NP_001276674.1:n.-95A>C
NM_002046.5:c.-24+21A>C	NP_002037.2:n.-24+21A>C
NM_001289745.2:c.-95A>C	NP_001276674.1:n.-95A>C
NM_001357943.1:c.-24+21A>C	NP_001344872.1:n.-24+21A>C
NM_002046.6:c.-24+21A>C	NP_002037.2:n.-24+21A>C
NR_152150.1:n.53+21A>C
NM_002046.7:c.-24+21A>C MANE Select	NP_002037.2:n.-24+21A>C
NM_001289745.3:c.-95A>C	NP_001276674.1:n.-95A>C
NM_001289746.2:c.-243A>C	NP_001276675.1:n.-243A>C
NM_001357943.2:c.-24+21A>C	NP_001344872.1:n.-24+21A>C
NR_152150.2:n.53+21A>C