Canonical Allele Identifier: CA2187814869
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720521A= , CM000677.2:g.74720521A= GRCh38
NC_000015.9:g.75012862A= , CM000677.1:g.75012862A= GRCh37
NC_000015.8:g.72799915A= NCBI36
NG_008431.1:g.2980A=
NG_008431.2:g.2980A=
NG_061374.1:g.10008T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.1507T= MANE Select ENSP00000369050.3:p.Cys503=
ENST00000379727.7:c.1507T= ENSP00000369050.3:p.Cys503=
ENST00000395048.6:c.1507T= ENSP00000378488.2:p.Cys503=
ENST00000395049.8:c.1420T= ENSP00000378489.4:p.Cys474=
ENST00000567032.5:c.1507T= ENSP00000456585.1:p.Cys503=
ENST00000612821.4:c.1423T= ENSP00000479744.1:p.Cys475=
ENST00000617691.4:c.1420T= ENSP00000482863.1:p.Cys474=
NM_000499.3:c.1507T= NP_000490.1:p.Cys503=
XM_005254185.1:c.1507T= XP_005254242.1:p.Cys503=
NM_000499.5:c.1507T= NP_000490.1:p.Cys503=
NM_001319216.2:c.1420T= NP_001306145.1:p.Cys474=
NM_001319217.2:c.1507T= MANE Select NP_001306146.1:p.Cys503=