Canonical Allele Identifier: CA2629503237
Gene: CYP1A1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719851G>A , CM000677.2:g.74719851G>A GRCh38
NC_000015.9:g.75012192G>A , CM000677.1:g.75012192G>A GRCh37
NC_000015.8:g.72799245G>A NCBI36
NG_008431.1:g.2310G>A
NG_008431.2:g.2310G>A
NG_061374.1:g.10678C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*638C>T MANE Select ENSP00000369050.3:n.*638C>T
ENST00000379727.7:c.*638C>T ENSP00000369050.3:n.*638C>T
ENST00000395048.6:c.*638C>T ENSP00000378488.2:n.*638C>T
ENST00000612821.4:c.2093C>T ENSP00000479744.1:n.2093C>T
ENST00000617691.4:c.*638C>T ENSP00000482863.1:n.*638C>T
NM_000499.3:c.*638C>T NP_000490.1:n.*638C>T
XM_005254185.1:c.*638C>T XP_005254242.1:n.*638C>T
NM_000499.5:c.*638C>T NP_000490.1:n.*638C>T
NM_001319216.2:c.*638C>T NP_001306145.1:n.*638C>T
NM_001319217.2:c.*638C>T MANE Select NP_001306146.1:n.*638C>T