Canonical Allele Identifier: CA1929292120

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94941772_94941773delinsTA , CM000672.2:g.94941772_94941773delinsTA	GRCh38
NC_000010.10:g.96701529_96701530delinsTA , CM000672.1:g.96701529_96701530delinsTA	GRCh37
NC_000010.9:g.96691519_96691520delinsTA	NCBI36
NG_008385.1:g.8115_8116delinsTA
NG_008385.2:g.8615_8616delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.169-86_169-85delinsTA MANE Select	ENSP00000260682.6:n.169-86_169-85delinsTA
ENST00000643112.1:c.169-86_169-85delinsTA	ENSP00000496202.1:n.169-86_169-85delinsTA
ENST00000645207.1:n.236_237delinsTA
ENST00000260682.6:c.169-86_169-85delinsTA	ENSP00000260682.6:n.169-86_169-85delinsTA
ENST00000461906.1:n.194-86_194-85delinsTA
NM_000771.3:c.169-86_169-85delinsTA	NP_000762.2:n.169-86_169-85delinsTA
NM_000771.4:c.169-86_169-85delinsTA MANE Select	NP_000762.2:n.169-86_169-85delinsTA