Canonical Allele Identifier: CA2617278485

Gene: GAPDH

Linked Data

• gnomAD v4: 12-6534573-A-AGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.6534573_6534574insGCC , CM000674.2:g.6534573_6534574insGCC	GRCh38
NC_000012.11:g.6643739_6643740insGCC , CM000674.1:g.6643739_6643740insGCC	GRCh37
NC_000012.10:g.6514000_6514001insGCC	NCBI36
NG_007073.2:g.5083_5084insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000229239.10:c.-24+4_-24+5insGCC MANE Select	ENSP00000229239.5:n.-24+4_-24+5insGCC
ENST00000229239.9:c.-24+4_-24+5insGCC	ENSP00000229239.5:n.-24+4_-24+5insGCC
ENST00000396856.5:c.-276+4_-276+5insGCC	ENSP00000380065.1:n.-276+4_-276+5insGCC
ENST00000396861.5:c.-112_-111insGCC	ENSP00000380070.1:n.-112_-111insGCC
ENST00000474249.5:n.29+4_29+5insGCC
ENST00000492719.5:n.37+4_37+5insGCC
ENST00000496049.1:n.58+4_58+5insGCC
NM_001289745.1:c.-112_-111insGCC	NP_001276674.1:n.-112_-111insGCC
NM_002046.5:c.-24+4_-24+5insGCC	NP_002037.2:n.-24+4_-24+5insGCC
NM_001289745.2:c.-112_-111insGCC	NP_001276674.1:n.-112_-111insGCC
NM_001357943.1:c.-24+4_-24+5insGCC	NP_001344872.1:n.-24+4_-24+5insGCC
NM_002046.6:c.-24+4_-24+5insGCC	NP_002037.2:n.-24+4_-24+5insGCC
NR_152150.1:n.53+4_53+5insGCC
NM_002046.7:c.-24+4_-24+5insGCC MANE Select	NP_002037.2:n.-24+4_-24+5insGCC
NM_001289745.3:c.-112_-111insGCC	NP_001276674.1:n.-112_-111insGCC
NM_001289746.2:c.-260_-259insGCC	NP_001276675.1:n.-260_-259insGCC
NM_001357943.2:c.-24+4_-24+5insGCC	NP_001344872.1:n.-24+4_-24+5insGCC
NR_152150.2:n.53+4_53+5insGCC