Canonical Allele Identifier: CA2014120607
Gene: GAPDH HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534589A= , CM000674.2:g.6534589A= GRCh38
NC_000012.11:g.6643755A= , CM000674.1:g.6643755A= GRCh37
NC_000012.10:g.6514016A= NCBI36
NG_007073.2:g.5099A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.10:c.-24+20A= MANE Select ENSP00000229239.5:n.-24+20A=
ENST00000229239.9:c.-24+20A= ENSP00000229239.5:n.-24+20A=
ENST00000396856.5:c.-276+20A= ENSP00000380065.1:n.-276+20A=
ENST00000396861.5:c.-96A= ENSP00000380070.1:n.-96A=
ENST00000474249.5:n.29+20A=
ENST00000492719.5:n.37+20A=
ENST00000496049.1:n.58+20A=
NM_001289745.1:c.-96A= NP_001276674.1:n.-96A=
NM_002046.5:c.-24+20A= NP_002037.2:n.-24+20A=
NM_001289745.2:c.-96A= NP_001276674.1:n.-96A=
NM_001357943.1:c.-24+20A= NP_001344872.1:n.-24+20A=
NM_002046.6:c.-24+20A= NP_002037.2:n.-24+20A=
NR_152150.1:n.53+20A=
NM_002046.7:c.-24+20A= MANE Select NP_002037.2:n.-24+20A=
NM_001289745.3:c.-96A= NP_001276674.1:n.-96A=
NM_001289746.2:c.-244A= NP_001276675.1:n.-244A=
NM_001357943.2:c.-24+20A= NP_001344872.1:n.-24+20A=
NR_152150.2:n.53+20A=