Canonical Allele Identifier: CA931402161

Gene: CYP2C9

Linked Data

• gnomAD v3: 10-94974526-A-ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
• gnomAD v4: 10-94974526-A-ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94974534_94974535insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.2:g.94974534_94974535insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh38
NC_000010.10:g.96734291_96734292insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT , CM000672.1:g.96734291_96734292insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	GRCh37
NC_000010.9:g.96724281_96724282insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NCBI36
NG_008385.1:g.40877_40878insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NG_008385.2:g.41377_41378insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000260682.6:n.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTT...
ENST00000643112.1:c.820-6649_820-6648insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000496202.1:n.820-6649_820-6648insTTTTTTTTTTTTTTTTTTTTT...
ENST00000260682.6:c.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000260682.6:n.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTT...
NM_000771.3:c.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_000762.2:n.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTTTTTTTT...
NM_000771.4:c.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_000762.2:n.961+2289_961+2290insTTTTTTTTTTTTTTTTTTTTTTTTTTT...