Canonical Allele Identifier: CA1929278198

Gene: CYP2C19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94849855_94849856delinsAC , CM000672.2:g.94849855_94849856delinsAC	GRCh38
NC_000010.10:g.96609612_96609613delinsAC , CM000672.1:g.96609612_96609613delinsAC	GRCh37
NC_000010.9:g.96599602_96599603delinsAC	NCBI36
NG_008384.2:g.92150_92151delinsAC
NG_008384.3:g.92175_92176delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.1150-62_1150-61delinsAC MANE Select	ENSP00000360372.3:n.1150-62_1150-61delinsAC
ENST00000645461.1:n.2061-62_2061-61delinsAC
ENST00000371321.7:c.1150-62_1150-61delinsAC	ENSP00000360372.3:n.1150-62_1150-61delinsAC
ENST00000464755.1:c.1913-62_1913-61delinsAC	ENSP00000483243.1:n.1913-62_1913-61delinsAC
NM_000769.2:c.1150-62_1150-61delinsAC	NP_000760.1:n.1150-62_1150-61delinsAC
NM_000769.4:c.1150-62_1150-61delinsAC MANE Select	NP_000760.1:n.1150-62_1150-61delinsAC