Canonical Allele Identifier: CA2617278612

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534650-C-CGCCGCTGCGGGGTGGGCCCGGGCG

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534654_6534677dup , CM000674.2:g.6534654_6534677dup	GRCh38
NC_000012.11:g.6643820_6643843dup , CM000674.1:g.6643820_6643843dup	GRCh37
NC_000012.10:g.6514081_6514104dup	NCBI36
NG_007073.2:g.5164_5187dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000229239.10:c.-24+85_-24+108dup MANE Select	ENSP00000229239.5:n.-24+85_-24+108dup
ENST00000229239.9:c.-24+85_-24+108dup	ENSP00000229239.5:n.-24+85_-24+108dup
ENST00000396856.5:c.-276+85_-276+108dup	ENSP00000380065.1:n.-276+85_-276+108dup
ENST00000396861.5:c.-31_-24+16dup
ENST00000474249.5:n.29+85_29+108dup
ENST00000492719.5:n.37+85_37+108dup
ENST00000496049.1:n.58+85_58+108dup
NM_001289745.1:c.-31_-24+16dup
NM_002046.5:c.-24+85_-24+108dup	NP_002037.2:n.-24+85_-24+108dup
NM_001289745.2:c.-31_-24+16dup
NM_001357943.1:c.-24+85_-24+108dup	NP_001344872.1:n.-24+85_-24+108dup
NM_002046.6:c.-24+85_-24+108dup	NP_002037.2:n.-24+85_-24+108dup
NR_152150.1:n.53+85_53+108dup
NM_002046.7:c.-24+85_-24+108dup MANE Select	NP_002037.2:n.-24+85_-24+108dup
NM_001289745.3:c.-31_-24+16dup
NM_001289746.2:c.-179_-156dup	NP_001276675.1:n.-179_-156dup
NM_001357943.2:c.-24+85_-24+108dup	NP_001344872.1:n.-24+85_-24+108dup
NR_152150.2:n.53+85_53+108dup