Canonical Allele Identifier: CA2187827037
Gene: CYP1A2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74754798_74754799delinsTG , CM000677.2:g.74754798_74754799delinsTG GRCh38
NC_000015.9:g.75047139_75047140delinsTG , CM000677.1:g.75047139_75047140delinsTG GRCh37
NC_000015.8:g.72834192_72834193delinsTG NCBI36
NG_008431.1:g.37257_37258delinsTG
NG_008431.2:g.37257_37258delinsTG
NG_061543.1:g.10954_10955delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000343932.5:c.1261_1262delinsTG MANE Select ENSP00000342007.4:p.Trp421=
ENST00000343932.4:c.1261_1262delinsTG ENSP00000342007.4:p.Trp421=
NM_000761.4:c.1261_1262delinsTG NP_000752.2:p.Trp421=
NM_000761.5:c.1261_1262delinsTG MANE Select NP_000752.2:p.Trp421=