Canonical Allele Identifier: CA2187814520
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719673A= , CM000677.2:g.74719673A= GRCh38
NC_000015.9:g.75012014A= , CM000677.1:g.75012014A= GRCh37
NC_000015.8:g.72799067A= NCBI36
NG_008431.1:g.2132A=
NG_008431.2:g.2132A=
NG_061374.1:g.10856T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*816T= MANE Select ENSP00000369050.3:n.*816T=
ENST00000379727.7:c.*816T= ENSP00000369050.3:n.*816T=
ENST00000395048.6:c.*816T= ENSP00000378488.2:n.*816T=
ENST00000612821.4:c.2271T= ENSP00000479744.1:n.2271T=
ENST00000617691.4:c.*816T= ENSP00000482863.1:n.*816T=
NM_000499.3:c.*816T= NP_000490.1:n.*816T=
XM_005254185.1:c.*816T= XP_005254242.1:n.*816T=
NM_000499.5:c.*816T= NP_000490.1:n.*816T=
NM_001319216.2:c.*816T= NP_001306145.1:n.*816T=
NM_001319217.2:c.*816T= MANE Select NP_001306146.1:n.*816T=