Canonical Allele Identifier: CA2617278563
Gene: GAPDH HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6534633_6534698dup , CM000674.2:g.6534633_6534698dup GRCh38
NC_000012.11:g.6643799_6643864dup , CM000674.1:g.6643799_6643864dup GRCh37
NC_000012.10:g.6514060_6514125dup NCBI36
NG_007073.2:g.5143_5208dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000229239.10:c.-24+64_-23-112dup MANE Select ENSP00000229239.5:n.-24+64_-23-112dup
ENST00000229239.9:c.-24+64_-23-112dup ENSP00000229239.5:n.-24+64_-23-112dup
ENST00000396856.5:c.-276+64_-275-112dup ENSP00000380065.1:n.-276+64_-275-112dup
ENST00000396861.5:c.-52_-24+37dup
ENST00000474249.5:n.29+64_30-112dup
ENST00000492719.5:n.37+64_38-112dup
ENST00000496049.1:n.58+64_59-112dup
NM_001289745.1:c.-52_-24+37dup
NM_002046.5:c.-24+64_-23-112dup NP_002037.2:n.-24+64_-23-112dup
NM_001289745.2:c.-52_-24+37dup
NM_001357943.1:c.-24+64_-23-112dup NP_001344872.1:n.-24+64_-23-112dup
NM_002046.6:c.-24+64_-23-112dup NP_002037.2:n.-24+64_-23-112dup
NR_152150.1:n.53+64_54-112dup
NM_002046.7:c.-24+64_-23-112dup MANE Select NP_002037.2:n.-24+64_-23-112dup
NM_001289745.3:c.-52_-24+37dup
NM_001289746.2:c.-200_-135dup NP_001276675.1:n.-200_-135dup
NM_001357943.2:c.-24+64_-23-112dup NP_001344872.1:n.-24+64_-23-112dup
NR_152150.2:n.53+64_54-112dup