Canonical Allele Identifier: CA232399912

Gene: GAPDH

Linked Data

• dbSNP Id: rs987030923
• MyVariant Identifiers: chr12:g.6643746G>A (hg19) ; chr12:g.6534580G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534580G>A , CM000674.2:g.6534580G>A	GRCh38
NC_000012.11:g.6643746G>A , CM000674.1:g.6643746G>A	GRCh37
NC_000012.10:g.6514007G>A	NCBI36
NG_007073.2:g.5090G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.-24+11G>A MANE Select	ENSP00000229239.5:n.-24+11G>A
ENST00000229239.9:c.-24+11G>A	ENSP00000229239.5:n.-24+11G>A
ENST00000396856.5:c.-276+11G>A	ENSP00000380065.1:n.-276+11G>A
ENST00000396861.5:c.-105G>A	ENSP00000380070.1:n.-105G>A
ENST00000474249.5:n.29+11G>A
ENST00000492719.5:n.37+11G>A
ENST00000496049.1:n.58+11G>A
NM_001289745.1:c.-105G>A	NP_001276674.1:n.-105G>A
NM_002046.5:c.-24+11G>A	NP_002037.2:n.-24+11G>A
NM_001289745.2:c.-105G>A	NP_001276674.1:n.-105G>A
NM_001357943.1:c.-24+11G>A	NP_001344872.1:n.-24+11G>A
NM_002046.6:c.-24+11G>A	NP_002037.2:n.-24+11G>A
NR_152150.1:n.53+11G>A
NM_002046.7:c.-24+11G>A MANE Select	NP_002037.2:n.-24+11G>A
NM_001289745.3:c.-105G>A	NP_001276674.1:n.-105G>A
NM_001289746.2:c.-253G>A	NP_001276675.1:n.-253G>A
NM_001357943.2:c.-24+11G>A	NP_001344872.1:n.-24+11G>A
NR_152150.2:n.53+11G>A