Canonical Allele Identifier: CA603118192

Gene: GAPDH

Linked Data

• dbSNP Id: rs1488241918
• gnomAD v2: 12-6643800-A-G
• gnomAD v3: 12-6534634-A-G
• gnomAD v4: 12-6534634-A-G
• MyVariant Identifiers: chr12:g.6643800A>G (hg19) ; chr12:g.6534634A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534634A>G , CM000674.2:g.6534634A>G	GRCh38
NC_000012.11:g.6643800A>G , CM000674.1:g.6643800A>G	GRCh37
NC_000012.10:g.6514061A>G	NCBI36
NG_007073.2:g.5144A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+65A>G MANE Select	ENSP00000229239.5:n.-24+65A>G
ENST00000229239.9:c.-24+65A>G	ENSP00000229239.5:n.-24+65A>G
ENST00000396856.5:c.-276+65A>G	ENSP00000380065.1:n.-276+65A>G
ENST00000396861.5:c.-51A>G	ENSP00000380070.1:n.-51A>G
ENST00000474249.5:n.29+65A>G
ENST00000492719.5:n.37+65A>G
ENST00000496049.1:n.58+65A>G
NM_001289745.1:c.-51A>G	NP_001276674.1:n.-51A>G
NM_002046.5:c.-24+65A>G	NP_002037.2:n.-24+65A>G
NM_001289745.2:c.-51A>G	NP_001276674.1:n.-51A>G
NM_001357943.1:c.-24+65A>G	NP_001344872.1:n.-24+65A>G
NM_002046.6:c.-24+65A>G	NP_002037.2:n.-24+65A>G
NR_152150.1:n.53+65A>G
NM_002046.7:c.-24+65A>G MANE Select	NP_002037.2:n.-24+65A>G
NM_001289745.3:c.-51A>G	NP_001276674.1:n.-51A>G
NM_001289746.2:c.-199A>G	NP_001276675.1:n.-199A>G
NM_001357943.2:c.-24+65A>G	NP_001344872.1:n.-24+65A>G
NR_152150.2:n.53+65A>G