Canonical Allele Identifier: CA1929222915

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94782213_94782214delinsTA , CM000672.2:g.94782213_94782214delinsTA	GRCh38
NC_000010.10:g.96541970_96541971delinsTA , CM000672.1:g.96541970_96541971delinsTA	GRCh37
NC_000010.9:g.96531960_96531961delinsTA	NCBI36
NG_008384.2:g.24508_24509delinsTA
NG_008384.3:g.24533_24534delinsTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.819+216_819+217delinsTA MANE Select	ENSP00000360372.3:n.819+216_819+217delinsTA
ENST00000645461.1:n.1872+216_1872+217delinsTA
ENST00000371321.7:c.819+216_819+217delinsTA	ENSP00000360372.3:n.819+216_819+217delinsTA
ENST00000464755.1:c.1582+216_1582+217delinsTA	ENSP00000483243.1:n.1582+216_1582+217delinsTA
NM_000769.2:c.819+216_819+217delinsTA	NP_000760.1:n.819+216_819+217delinsTA
NM_000769.4:c.819+216_819+217delinsTA MANE Select	NP_000760.1:n.819+216_819+217delinsTA