Canonical Allele Identifier: CA1929292286

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94942055_94942056delinsTG , CM000672.2:g.94942055_94942056delinsTG	GRCh38
NC_000010.10:g.96701812_96701813delinsTG , CM000672.1:g.96701812_96701813delinsTG	GRCh37
NC_000010.9:g.96691802_96691803delinsTG	NCBI36
NG_008385.1:g.8398_8399delinsTG
NG_008385.2:g.8898_8899delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.331+35_331+36delinsTG MANE Select	ENSP00000260682.6:n.331+35_331+36delinsTG
ENST00000643112.1:c.331+35_331+36delinsTG	ENSP00000496202.1:n.331+35_331+36delinsTG
ENST00000645207.1:n.484+35_484+36delinsTG
ENST00000260682.6:c.331+35_331+36delinsTG	ENSP00000260682.6:n.331+35_331+36delinsTG
ENST00000461906.1:n.356+35_356+36delinsTG
ENST00000473496.1:n.102+35_102+36delinsTG
NM_000771.3:c.331+35_331+36delinsTG	NP_000762.2:n.331+35_331+36delinsTG
NM_000771.4:c.331+35_331+36delinsTG MANE Select	NP_000762.2:n.331+35_331+36delinsTG