Canonical Allele Identifier: CA1929218218

Gene: CYP2C19 MTND4P19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94774400_94774418delinsAATAAGCTATAAACTCTGT , CM000672.2:g.94774400_94774418delinsAATAAGCTATAAACTCTGT	GRCh38
NC_000010.10:g.96534157_96534175delinsAATAAGCTATAAACTCTGT , CM000672.1:g.96534157_96534175delinsAATAAGCTATAAACTCTGT	GRCh37
NC_000010.9:g.96524147_96524165delinsAATAAGCTATAAACTCTGT	NCBI36
NG_008384.2:g.16695_16713delinsAATAAGCTATAAACTCTGT
NG_008384.3:g.16720_16738delinsAATAAGCTATAAACTCTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.169-658_169-640delinsAATAAGCTATAAACTCTGT (CYP2C19) MANE Select	ENSP00000360372.3:n.169-658_169-640delinsAATAAGCTATAAACTCTGT
ENST00000645461.1:n.564_582delinsAATAAGCTATAAACTCTGT (CYP2C19)
ENST00000371321.7:c.169-658_169-640delinsAATAAGCTATAAACTCTGT (CYP2C19)	ENSP00000360372.3:n.169-658_169-640delinsAATAAGCTATAAACTCTGT
ENST00000446659.1:n.216_234delinsACAGAGTTTATAGCTTATT (MTND4P19)
ENST00000464755.1:c.932-658_932-640delinsAATAAGCTATAAACTCTGT	ENSP00000483243.1:n.932-658_932-640delinsAATAAGCTATAAACTCTGT
ENST00000480405.2:c.169-658_169-640delinsAATAAGCTATAAACTCTGT (CYP2C19)	ENSP00000483847.1:n.169-658_169-640delinsAATAAGCTATAAACTCTGT
NM_000769.2:c.169-658_169-640delinsAATAAGCTATAAACTCTGT (CYP2C19)	NP_000760.1:n.169-658_169-640delinsAATAAGCTATAAACTCTGT
NM_000769.4:c.169-658_169-640delinsAATAAGCTATAAACTCTGT (CYP2C19) MANE Select	NP_000760.1:n.169-658_169-640delinsAATAAGCTATAAACTCTGT