Canonical Allele Identifier: CA1929218227

Gene: CYP2C19 MTND4P19

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94774417_94774418delinsGT , CM000672.2:g.94774417_94774418delinsGT	GRCh38
NC_000010.10:g.96534174_96534175delinsGT , CM000672.1:g.96534174_96534175delinsGT	GRCh37
NC_000010.9:g.96524164_96524165delinsGT	NCBI36
NG_008384.2:g.16712_16713delinsGT
NG_008384.3:g.16737_16738delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371321.9:c.169-641_169-640delinsGT (CYP2C19) MANE Select	ENSP00000360372.3:n.169-641_169-640delinsGT
ENST00000645461.1:n.581_582delinsGT (CYP2C19)
ENST00000371321.7:c.169-641_169-640delinsGT (CYP2C19)	ENSP00000360372.3:n.169-641_169-640delinsGT
ENST00000446659.1:n.216_217delinsAC (MTND4P19)
ENST00000464755.1:c.932-641_932-640delinsGT	ENSP00000483243.1:n.932-641_932-640delinsGT
ENST00000480405.2:c.169-641_169-640delinsGT (CYP2C19)	ENSP00000483847.1:n.169-641_169-640delinsGT
NM_000769.2:c.169-641_169-640delinsGT (CYP2C19)	NP_000760.1:n.169-641_169-640delinsGT
NM_000769.4:c.169-641_169-640delinsGT (CYP2C19) MANE Select	NP_000760.1:n.169-641_169-640delinsGT