Canonical Allele Identifier: CA2617278632
Gene: GAPDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534663_6534692del , CM000674.2:g.6534663_6534692del GRCh38
NC_000012.11:g.6643829_6643858del , CM000674.1:g.6643829_6643858del GRCh37
NC_000012.10:g.6514090_6514119del NCBI36
NG_007073.2:g.5173_5202del

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.10:c.-24+94_-23-118del MANE Select ENSP00000229239.5:n.-24+94_-23-118del
ENST00000229239.9:c.-24+94_-23-118del ENSP00000229239.5:n.-24+94_-23-118del
ENST00000396856.5:c.-276+94_-275-118del ENSP00000380065.1:n.-276+94_-275-118del
ENST00000396861.5:c.-24+2_-24+31del
ENST00000474249.5:n.29+94_30-118del
ENST00000492719.5:n.37+94_38-118del
ENST00000496049.1:n.58+94_59-118del
NM_001289745.1:c.-24+2_-24+31del
NM_001289746.1:c.-170_-141del NP_001276675.1:n.-170_-141del
NM_002046.5:c.-24+94_-23-118del NP_002037.2:n.-24+94_-23-118del
NM_001289745.2:c.-24+2_-24+31del
NM_001357943.1:c.-24+94_-23-118del NP_001344872.1:n.-24+94_-23-118del
NM_002046.6:c.-24+94_-23-118del NP_002037.2:n.-24+94_-23-118del
NR_152150.1:n.53+94_54-118del
NM_002046.7:c.-24+94_-23-118del MANE Select NP_002037.2:n.-24+94_-23-118del
NM_001289745.3:c.-24+2_-24+31del
NM_001289746.2:c.-170_-141del NP_001276675.1:n.-170_-141del
NM_001357943.2:c.-24+94_-23-118del NP_001344872.1:n.-24+94_-23-118del
NR_152150.2:n.53+94_54-118del