Canonical Allele Identifier: CA2789064299

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94775535del , CM000672.2:g.94775535del	GRCh38
NC_000010.10:g.96535292del , CM000672.1:g.96535292del	GRCh37
NC_000010.9:g.96525282del	NCBI36
NG_008384.2:g.17830del
NG_008384.3:g.17855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.477del MANE Select	ENSP00000360372.3:p.Lys160ArgfsTer18
ENST00000645461.1:n.1530del
ENST00000371321.7:c.477del	ENSP00000360372.3:p.Lys160ArgfsTer18
ENST00000464755.1:c.1240del	ENSP00000483243.1:n.1240del
ENST00000480405.2:c.477del	ENSP00000483847.1:p.Lys160ArgfsTer10
NM_000769.2:c.477del	NP_000760.1:p.Lys160ArgfsTer18
NM_000769.4:c.477del MANE Select	NP_000760.1:p.Lys160ArgfsTer18