Canonical Allele Identifier: CA2596105776
Gene: CYP1A1 HGNC NCBI

Linked Data

dbSNP Id: rs2141712395

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719716del , CM000677.2:g.74719716del GRCh38
NC_000015.9:g.75012057del , CM000677.1:g.75012057del GRCh37
NC_000015.8:g.72799110del NCBI36
NG_008431.1:g.2175del
NG_008431.2:g.2175del
NG_061374.1:g.10817del

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*777del MANE Select ENSP00000369050.3:n.*777del
ENST00000379727.7:c.*777del ENSP00000369050.3:n.*777del
ENST00000395048.6:c.*777del ENSP00000378488.2:n.*777del
ENST00000612821.4:c.2232del ENSP00000479744.1:n.2232del
ENST00000617691.4:c.*777del ENSP00000482863.1:n.*777del
NM_000499.3:c.*777del NP_000490.1:n.*777del
XM_005254185.1:c.*777del XP_005254242.1:n.*777del
NM_000499.5:c.*777del NP_000490.1:n.*777del
NM_001319216.2:c.*777del NP_001306145.1:n.*777del
NM_001319217.2:c.*777del MANE Select NP_001306146.1:n.*777del