Canonical Allele Identifier: CA2610268149

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942746-A-ATTCTC

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942747_94942748insTCTCT , CM000672.2:g.94942747_94942748insTCTCT	GRCh38
NC_000010.10:g.96702504_96702505insTCTCT , CM000672.1:g.96702504_96702505insTCTCT	GRCh37
NC_000010.9:g.96692494_96692495insTCTCT	NCBI36
NG_008385.1:g.9090_9091insTCTCT
NG_008385.2:g.9590_9591insTCTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+406_481+407insTCTCT MANE Select	ENSP00000260682.6:n.481+406_481+407insTCTCT
ENST00000643112.1:c.481+406_481+407insTCTCT	ENSP00000496202.1:n.481+406_481+407insTCTCT
ENST00000645207.1:n.634+406_634+407insTCTCT
ENST00000260682.6:c.481+406_481+407insTCTCT	ENSP00000260682.6:n.481+406_481+407insTCTCT
ENST00000461906.1:n.912_913insTCTCT
ENST00000473496.1:n.252+406_252+407insTCTCT
NM_000771.3:c.481+406_481+407insTCTCT	NP_000762.2:n.481+406_481+407insTCTCT
NM_000771.4:c.481+406_481+407insTCTCT MANE Select	NP_000762.2:n.481+406_481+407insTCTCT