Canonical Allele Identifier: CA2610268145

Gene: CYP2C9

Linked Data

• gnomAD v4: 10-94942744-A-ACCATGTTGACTTGTCAAG

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942744_94942745insCCATGTTGACTTGTCAAG , CM000672.2:g.94942744_94942745insCCATGTTGACTTGTCAAG	GRCh38
NC_000010.10:g.96702501_96702502insCCATGTTGACTTGTCAAG , CM000672.1:g.96702501_96702502insCCATGTTGACTTGTCAAG	GRCh37
NC_000010.9:g.96692491_96692492insCCATGTTGACTTGTCAAG	NCBI36
NG_008385.1:g.9087_9088insCCATGTTGACTTGTCAAG
NG_008385.2:g.9587_9588insCCATGTTGACTTGTCAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.481+403_481+404insCCATGTTGACTTGTCAAG MANE Select	ENSP00000260682.6:n.481+403_481+404insCCATGTTGACTTGTCAAG
ENST00000643112.1:c.481+403_481+404insCCATGTTGACTTGTCAAG	ENSP00000496202.1:n.481+403_481+404insCCATGTTGACTTGTCAAG
ENST00000645207.1:n.634+403_634+404insCCATGTTGACTTGTCAAG
ENST00000260682.6:c.481+403_481+404insCCATGTTGACTTGTCAAG	ENSP00000260682.6:n.481+403_481+404insCCATGTTGACTTGTCAAG
ENST00000461906.1:n.909_910insCCATGTTGACTTGTCAAG
ENST00000473496.1:n.252+403_252+404insCCATGTTGACTTGTCAAG
NM_000771.3:c.481+403_481+404insCCATGTTGACTTGTCAAG	NP_000762.2:n.481+403_481+404insCCATGTTGACTTGTCAAG
NM_000771.4:c.481+403_481+404insCCATGTTGACTTGTCAAG MANE Select	NP_000762.2:n.481+403_481+404insCCATGTTGACTTGTCAAG