Canonical Allele Identifier: CA2187814773
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74720327G= , CM000677.2:g.74720327G= GRCh38
NC_000015.9:g.75012668G= , CM000677.1:g.75012668G= GRCh37
NC_000015.8:g.72799721G= NCBI36
NG_008431.1:g.2786G=
NG_008431.2:g.2786G=
NG_061374.1:g.10202C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*162C= MANE Select ENSP00000369050.3:n.*162C=
ENST00000379727.7:c.*162C= ENSP00000369050.3:n.*162C=
ENST00000395048.6:c.*162C= ENSP00000378488.2:n.*162C=
ENST00000567032.5:c.*162C= ENSP00000456585.1:n.*162C=
ENST00000612821.4:c.1617C= ENSP00000479744.1:n.1617C=
ENST00000617691.4:c.*162C= ENSP00000482863.1:n.*162C=
NM_000499.3:c.*162C= NP_000490.1:n.*162C=
XM_005254185.1:c.*162C= XP_005254242.1:n.*162C=
NM_000499.5:c.*162C= NP_000490.1:n.*162C=
NM_001319216.2:c.*162C= NP_001306145.1:n.*162C=
NM_001319217.2:c.*162C= MANE Select NP_001306146.1:n.*162C=