Canonical Allele Identifier: CA2617278686

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534686-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534686G>A , CM000674.2:g.6534686G>A	GRCh38
NC_000012.11:g.6643852G>A , CM000674.1:g.6643852G>A	GRCh37
NC_000012.10:g.6514113G>A	NCBI36
NG_007073.2:g.5196G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+117G>A MANE Select	ENSP00000229239.5:n.-24+117G>A
ENST00000229239.9:c.-24+117G>A	ENSP00000229239.5:n.-24+117G>A
ENST00000396856.5:c.-276+117G>A	ENSP00000380065.1:n.-276+117G>A
ENST00000396861.5:c.-24+25G>A	ENSP00000380070.1:n.-24+25G>A
ENST00000474249.5:n.29+117G>A
ENST00000492719.5:n.37+117G>A
ENST00000496049.1:n.58+117G>A
NM_001289745.1:c.-24+25G>A	NP_001276674.1:n.-24+25G>A
NM_001289746.1:c.-147G>A	NP_001276675.1:n.-147G>A
NM_002046.5:c.-24+117G>A	NP_002037.2:n.-24+117G>A
NM_001289745.2:c.-24+25G>A	NP_001276674.1:n.-24+25G>A
NM_001357943.1:c.-24+117G>A	NP_001344872.1:n.-24+117G>A
NM_002046.6:c.-24+117G>A	NP_002037.2:n.-24+117G>A
NR_152150.1:n.53+117G>A
NM_002046.7:c.-24+117G>A MANE Select	NP_002037.2:n.-24+117G>A
NM_001289745.3:c.-24+25G>A	NP_001276674.1:n.-24+25G>A
NM_001289746.2:c.-147G>A	NP_001276675.1:n.-147G>A
NM_001357943.2:c.-24+117G>A	NP_001344872.1:n.-24+117G>A
NR_152150.2:n.53+117G>A