Canonical Allele Identifier: CA2629502908
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719762G>A , CM000677.2:g.74719762G>A GRCh38
NC_000015.9:g.75012103G>A , CM000677.1:g.75012103G>A GRCh37
NC_000015.8:g.72799156G>A NCBI36
NG_008431.1:g.2221G>A
NG_008431.2:g.2221G>A
NG_061374.1:g.10767C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*727C>T MANE Select ENSP00000369050.3:n.*727C>T
ENST00000379727.7:c.*727C>T ENSP00000369050.3:n.*727C>T
ENST00000395048.6:c.*727C>T ENSP00000378488.2:n.*727C>T
ENST00000612821.4:c.2182C>T ENSP00000479744.1:n.2182C>T
ENST00000617691.4:c.*727C>T ENSP00000482863.1:n.*727C>T
NM_000499.3:c.*727C>T NP_000490.1:n.*727C>T
XM_005254185.1:c.*727C>T XP_005254242.1:n.*727C>T
NM_000499.5:c.*727C>T NP_000490.1:n.*727C>T
NM_001319216.2:c.*727C>T NP_001306145.1:n.*727C>T
NM_001319217.2:c.*727C>T MANE Select NP_001306146.1:n.*727C>T