Canonical Allele Identifier: CA2741120235
Gene: CYP2C19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.94762710_94762711dup , CM000672.2:g.94762710_94762711dup GRCh38
NC_000010.10:g.96522467_96522468dup , CM000672.1:g.96522467_96522468dup GRCh37
NC_000010.9:g.96512457_96512458dup NCBI36
NG_008384.2:g.5005_5006dup
NG_008384.3:g.5030_5031dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371321.9:c.5_6dup MANE Select ENSP00000360372.3:p.Pro3IlefsTer?
ENST00000371321.7:c.5_6dup ENSP00000360372.3:p.Pro3IlefsTer?
ENST00000464755.1:c.932-12348_932-12347dup ENSP00000483243.1:n.932-12348_932-12347du...
ENST00000480405.2:c.5_6dup ENSP00000483847.1:p.Pro3IlefsTer?
NM_000769.2:c.5_6dup NP_000760.1:p.Pro3IlefsTer?
NM_000769.4:c.5_6dup MANE Select NP_000760.1:p.Pro3IlefsTer?