Canonical Allele Identifier: CA653552641

Gene: CYP2C19

Linked Data

• COSMIC: COSN15661618

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94852987_94852988insA , CM000672.2:g.94852987_94852988insA	GRCh38
NC_000010.10:g.96612744_96612745insA , CM000672.1:g.96612744_96612745insA	GRCh37
NC_000010.9:g.96602734_96602735insA	NCBI36
NG_008384.2:g.95282_95283insA
NG_008384.3:g.95307_95308insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.*73_*74insA MANE Select	ENSP00000360372.3:n.*73_*74insA
ENST00000645461.1:n.2457_2458insA
ENST00000371321.7:c.*73_*74insA	ENSP00000360372.3:n.*73_*74insA
ENST00000464755.1:c.2309_2310insA	ENSP00000483243.1:n.2309_2310insA
NM_000769.2:c.*73_*74insA	NP_000760.1:n.*73_*74insA
NM_000769.4:c.*73_*74insA MANE Select	NP_000760.1:n.*73_*74insA