Canonical Allele Identifier: CA653585460

Gene: CYP2C19

Linked Data

• COSMIC: COSN18823550

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94762693_94762694insA , CM000672.2:g.94762693_94762694insA	GRCh38
NC_000010.10:g.96522450_96522451insA , CM000672.1:g.96522450_96522451insA	GRCh37
NC_000010.9:g.96512440_96512441insA	NCBI36
NG_008384.2:g.4988_4989insA
NG_008384.3:g.5013_5014insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.-13_-12insA MANE Select	ENSP00000360372.3:n.-13_-12insA
ENST00000371321.7:c.-13_-12insA	ENSP00000360372.3:n.-13_-12insA
ENST00000464755.1:c.932-12365_932-12364insA	ENSP00000483243.1:n.932-12365_932-12364insA
ENST00000480405.2:c.-13_-12insA	ENSP00000483847.1:n.-13_-12insA
NM_000769.2:c.-13_-12insA	NP_000760.1:n.-13_-12insA
NM_000769.4:c.-13_-12insA MANE Select	NP_000760.1:n.-13_-12insA