Canonical Allele Identifier: CA2542271044

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852587_94852588insG , CM000672.2:g.94852587_94852588insG	GRCh38
NC_000010.10:g.96612344_96612345insG , CM000672.1:g.96612344_96612345insG	GRCh37
NC_000010.9:g.96602334_96602335insG	NCBI36
NG_008384.2:g.94882_94883insG
NG_008384.3:g.94907_94908insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1292-146_1292-145insG MANE Select	ENSP00000360372.3:n.1292-146_1292-145insG
ENST00000645461.1:n.2203-146_2203-145insG
ENST00000371321.7:c.1292-146_1292-145insG	ENSP00000360372.3:n.1292-146_1292-145insG
ENST00000464755.1:c.2055-146_2055-145insG	ENSP00000483243.1:n.2055-146_2055-145insG
NM_000769.2:c.1292-146_1292-145insG	NP_000760.1:n.1292-146_1292-145insG
NM_000769.4:c.1292-146_1292-145insG MANE Select	NP_000760.1:n.1292-146_1292-145insG