Canonical Allele Identifier: CA1929218872

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775581_94775584delinsTCTC , CM000672.2:g.94775581_94775584delinsTCTC	GRCh38
NC_000010.10:g.96535338_96535341delinsTCTC , CM000672.1:g.96535338_96535341delinsTCTC	GRCh37
NC_000010.9:g.96525328_96525331delinsTCTC	NCBI36
NG_008384.2:g.17876_17879delinsTCTC
NG_008384.3:g.17901_17904delinsTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.481+42_481+45delinsTCTC MANE Select	ENSP00000360372.3:n.481+42_481+45delinsTCTC
ENST00000645461.1:n.1534+42_1534+45delinsTCTC
ENST00000371321.7:c.481+42_481+45delinsTCTC	ENSP00000360372.3:n.481+42_481+45delinsTCTC
ENST00000464755.1:c.1244+42_1244+45delinsTCTC	ENSP00000483243.1:n.1244+42_1244+45delinsTCTC
ENST00000480405.2:c.*34_*37delinsTCTC	ENSP00000483847.1:n.*34_*37delinsTCTC
NM_000769.2:c.481+42_481+45delinsTCTC	NP_000760.1:n.481+42_481+45delinsTCTC
NM_000769.4:c.481+42_481+45delinsTCTC MANE Select	NP_000760.1:n.481+42_481+45delinsTCTC