Canonical Allele Identifier: CA2187814920
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720618G= , CM000677.2:g.74720618G= GRCh38
NC_000015.9:g.75012959G= , CM000677.1:g.75012959G= GRCh37
NC_000015.8:g.72800012G= NCBI36
NG_008431.1:g.3077G=
NG_008431.2:g.3077G=
NG_061374.1:g.9911C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.1410C= MANE Select ENSP00000369050.3:p.Phe470=
ENST00000379727.7:c.1410C= ENSP00000369050.3:p.Phe470=
ENST00000395048.6:c.1410C= ENSP00000378488.2:p.Phe470=
ENST00000395049.8:c.1323C= ENSP00000378489.4:p.Phe441=
ENST00000567032.5:c.1410C= ENSP00000456585.1:p.Phe470=
ENST00000612821.4:c.1326C= ENSP00000479744.1:p.Phe442=
ENST00000617691.4:c.1323C= ENSP00000482863.1:p.Phe441=
NM_000499.3:c.1410C= NP_000490.1:p.Phe470=
XM_005254185.1:c.1410C= XP_005254242.1:p.Phe470=
NM_000499.5:c.1410C= NP_000490.1:p.Phe470=
NM_001319216.2:c.1323C= NP_001306145.1:p.Phe441=
NM_001319217.2:c.1410C= MANE Select NP_001306146.1:p.Phe470=