Canonical Allele Identifier: CA2794420494
Gene: GAPDH HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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