Canonical Allele Identifier: CA2187814615
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719881G= , CM000677.2:g.74719881G= GRCh38
NC_000015.9:g.75012222G= , CM000677.1:g.75012222G= GRCh37
NC_000015.8:g.72799275G= NCBI36
NG_008431.1:g.2340G=
NG_008431.2:g.2340G=
NG_061374.1:g.10648C=

Transcript Alleles

HGVS Amino-acid change
ENST00000379727.8:c.*608C= MANE Select ENSP00000369050.3:n.*608C=
ENST00000379727.7:c.*608C= ENSP00000369050.3:n.*608C=
ENST00000395048.6:c.*608C= ENSP00000378488.2:n.*608C=
ENST00000612821.4:c.2063C= ENSP00000479744.1:n.2063C=
ENST00000617691.4:c.*608C= ENSP00000482863.1:n.*608C=
NM_000499.3:c.*608C= NP_000490.1:n.*608C=
XM_005254185.1:c.*608C= XP_005254242.1:n.*608C=
NM_000499.5:c.*608C= NP_000490.1:n.*608C=
NM_001319216.2:c.*608C= NP_001306145.1:n.*608C=
NM_001319217.2:c.*608C= MANE Select NP_001306146.1:n.*608C=