Canonical Allele Identifier: CA690978482

Gene: GAPDH

Linked Data

• dbSNP Id: rs1459946582
• gnomAD v4: 12-6534734-C-T
• MyVariant Identifiers: chr12:g.6643900C>T (hg19) ; chr12:g.6534734C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534734C>T , CM000674.2:g.6534734C>T	GRCh38
NC_000012.11:g.6643900C>T , CM000674.1:g.6643900C>T	GRCh37
NC_000012.10:g.6514161C>T	NCBI36
NG_007073.2:g.5244C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.-23-76C>T MANE Select	ENSP00000229239.5:n.-23-76C>T
ENST00000229239.9:c.-23-76C>T	ENSP00000229239.5:n.-23-76C>T
ENST00000396856.5:c.-275-76C>T	ENSP00000380065.1:n.-275-76C>T
ENST00000396861.5:c.-24+73C>T	ENSP00000380070.1:n.-24+73C>T
ENST00000474249.5:n.30-76C>T
ENST00000492719.5:n.38-76C>T
ENST00000496049.1:n.59-76C>T
NM_001289745.1:c.-24+73C>T	NP_001276674.1:n.-24+73C>T
NM_001289746.1:c.-99C>T	NP_001276675.1:n.-99C>T
NM_002046.5:c.-23-76C>T	NP_002037.2:n.-23-76C>T
NM_001289745.2:c.-24+73C>T	NP_001276674.1:n.-24+73C>T
NM_001357943.1:c.-23-76C>T	NP_001344872.1:n.-23-76C>T
NM_002046.6:c.-23-76C>T	NP_002037.2:n.-23-76C>T
NR_152150.1:n.54-76C>T
NM_002046.7:c.-23-76C>T MANE Select	NP_002037.2:n.-23-76C>T
NM_001289745.3:c.-24+73C>T	NP_001276674.1:n.-24+73C>T
NM_001289746.2:c.-99C>T	NP_001276675.1:n.-99C>T
NM_001357943.2:c.-23-76C>T	NP_001344872.1:n.-23-76C>T
NR_152150.2:n.54-76C>T