Canonical Allele Identifier: CA2187814608
Gene: CYP1A1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74719856C= , CM000677.2:g.74719856C= GRCh38
NC_000015.9:g.75012197C= , CM000677.1:g.75012197C= GRCh37
NC_000015.8:g.72799250C= NCBI36
NG_008431.1:g.2315C=
NG_008431.2:g.2315C=
NG_061374.1:g.10673G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.*633G= MANE Select ENSP00000369050.3:n.*633G=
ENST00000379727.7:c.*633G= ENSP00000369050.3:n.*633G=
ENST00000395048.6:c.*633G= ENSP00000378488.2:n.*633G=
ENST00000612821.4:c.2088G= ENSP00000479744.1:n.2088G=
ENST00000617691.4:c.*633G= ENSP00000482863.1:n.*633G=
NM_000499.3:c.*633G= NP_000490.1:n.*633G=
XM_005254185.1:c.*633G= XP_005254242.1:n.*633G=
NM_000499.5:c.*633G= NP_000490.1:n.*633G=
NM_001319216.2:c.*633G= NP_001306145.1:n.*633G=
NM_001319217.2:c.*633G= MANE Select NP_001306146.1:n.*633G=