Canonical Allele Identifier: CA2617278617

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534653-CGCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534656_6534658del , CM000674.2:g.6534656_6534658del	GRCh38
NC_000012.11:g.6643822_6643824del , CM000674.1:g.6643822_6643824del	GRCh37
NC_000012.10:g.6514083_6514085del	NCBI36
NG_007073.2:g.5166_5168del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+87_-24+89del MANE Select	ENSP00000229239.5:n.-24+87_-24+89del
ENST00000229239.9:c.-24+87_-24+89del	ENSP00000229239.5:n.-24+87_-24+89del
ENST00000396856.5:c.-276+87_-276+89del	ENSP00000380065.1:n.-276+87_-276+89del
ENST00000396861.5:c.-29_-27del	ENSP00000380070.1:n.-29_-27del
ENST00000474249.5:n.29+87_29+89del
ENST00000492719.5:n.37+87_37+89del
ENST00000496049.1:n.58+87_58+89del
NM_001289745.1:c.-29_-27del	NP_001276674.1:n.-29_-27del
NM_002046.5:c.-24+87_-24+89del	NP_002037.2:n.-24+87_-24+89del
NM_001289745.2:c.-29_-27del	NP_001276674.1:n.-29_-27del
NM_001357943.1:c.-24+87_-24+89del	NP_001344872.1:n.-24+87_-24+89del
NM_002046.6:c.-24+87_-24+89del	NP_002037.2:n.-24+87_-24+89del
NR_152150.1:n.53+87_53+89del
NM_002046.7:c.-24+87_-24+89del MANE Select	NP_002037.2:n.-24+87_-24+89del
NM_001289745.3:c.-29_-27del	NP_001276674.1:n.-29_-27del
NM_001289746.2:c.-177_-175del	NP_001276675.1:n.-177_-175del
NM_001357943.2:c.-24+87_-24+89del	NP_001344872.1:n.-24+87_-24+89del
NR_152150.2:n.53+87_53+89del