Canonical Allele Identifier: CA2529924439
Gene: CYP2C19 HGNC NCBI
MTND4P19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94774444del , CM000672.2:g.94774444del GRCh38
NC_000010.10:g.96534201del , CM000672.1:g.96534201del GRCh37
NC_000010.9:g.96524191del NCBI36
NG_008384.2:g.16739del
NG_008384.3:g.16764del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371321.9:c.169-614del (CYP2C19) MANE Select ENSP00000360372.3:n.169-614del
ENST00000645461.1:n.608del (CYP2C19)
ENST00000371321.7:c.169-614del (CYP2C19) ENSP00000360372.3:n.169-614del
ENST00000446659.1:n.190del (MTND4P19)
ENST00000464755.1:c.932-614del ENSP00000483243.1:n.932-614del
ENST00000480405.2:c.169-614del (CYP2C19) ENSP00000483847.1:n.169-614del
NM_000769.2:c.169-614del (CYP2C19) NP_000760.1:n.169-614del
NM_000769.4:c.169-614del (CYP2C19) MANE Select NP_000760.1:n.169-614del