Canonical Allele Identifier: CA2014120755
Gene: GAPDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534751G= , CM000674.2:g.6534751G= GRCh38
NC_000012.11:g.6643917G= , CM000674.1:g.6643917G= GRCh37
NC_000012.10:g.6514178G= NCBI36
NG_007073.2:g.5261G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.10:c.-23-59G= MANE Select ENSP00000229239.5:n.-23-59G=
ENST00000229239.9:c.-23-59G= ENSP00000229239.5:n.-23-59G=
ENST00000396856.5:c.-275-59G= ENSP00000380065.1:n.-275-59G=
ENST00000396861.5:c.-23-59G= ENSP00000380070.1:n.-23-59G=
ENST00000474249.5:n.30-59G=
ENST00000492719.5:n.38-59G=
ENST00000496049.1:n.59-59G=
NM_001289745.1:c.-23-59G= NP_001276674.1:n.-23-59G=
NM_001289746.1:c.-82G= NP_001276675.1:n.-82G=
NM_002046.5:c.-23-59G= NP_002037.2:n.-23-59G=
NM_001289745.2:c.-23-59G= NP_001276674.1:n.-23-59G=
NM_001357943.1:c.-23-59G= NP_001344872.1:n.-23-59G=
NM_002046.6:c.-23-59G= NP_002037.2:n.-23-59G=
NR_152150.1:n.54-59G=
NM_002046.7:c.-23-59G= MANE Select NP_002037.2:n.-23-59G=
NM_001289745.3:c.-23-59G= NP_001276674.1:n.-23-59G=
NM_001289746.2:c.-82G= NP_001276675.1:n.-82G=
NM_001357943.2:c.-23-59G= NP_001344872.1:n.-23-59G=
NR_152150.2:n.54-59G=