Canonical Allele Identifier: CA383602188
Gene: GAPDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534845A>T , CM000674.2:g.6534845A>T GRCh38
NC_000012.11:g.6644011A>T , CM000674.1:g.6644011A>T GRCh37
NC_000012.10:g.6514272A>T NCBI36
NG_007073.2:g.5355A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000229239.10:c.13A>T MANE Select ENSP00000229239.5:p.Lys5Ter
ENST00000229239.9:c.13A>T ENSP00000229239.5:p.Lys5Ter
ENST00000396856.5:c.-240A>T ENSP00000380065.1:n.-240A>T
ENST00000396859.5:c.13A>T ENSP00000380068.1:p.Lys5Ter
ENST00000396861.5:c.13A>T ENSP00000380070.1:p.Lys5Ter
ENST00000466525.1:n.54A>T
ENST00000466588.5:n.92A>T
ENST00000474249.5:n.65A>T
ENST00000492719.5:n.73A>T
ENST00000496049.1:n.94A>T
NM_001289745.1:c.13A>T NP_001276674.1:p.Lys5Ter
NM_001289746.1:c.13A>T NP_001276675.1:p.Lys5Ter
NM_002046.5:c.13A>T NP_002037.2:p.Lys5Ter
NM_001289745.2:c.13A>T NP_001276674.1:p.Lys5Ter
NM_001357943.1:c.13A>T NP_001344872.1:p.Lys5Ter
NM_002046.6:c.13A>T NP_002037.2:p.Lys5Ter
NR_152150.1:n.89A>T
NM_002046.7:c.13A>T MANE Select NP_002037.2:p.Lys5Ter
NM_001289745.3:c.13A>T NP_001276674.1:p.Lys5Ter
NM_001289746.2:c.13A>T NP_001276675.1:p.Lys5Ter
NM_001357943.2:c.13A>T NP_001344872.1:p.Lys5Ter
NR_152150.2:n.89A>T