Canonical Allele Identifier: CA272812848
Gene: CYP1A1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.74723851G>T , CM000677.2:g.74723851G>T GRCh38
NC_000015.9:g.75016192G>T , CM000677.1:g.75016192G>T GRCh37
NC_000015.8:g.72803245G>T NCBI36
NG_008431.1:g.6310G>T
NG_008431.2:g.6310G>T
NG_061374.1:g.6678C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379727.8:c.-29-725C>A MANE Select ENSP00000369050.3:n.-29-725C>A
ENST00000379727.7:c.-29-725C>A ENSP00000369050.3:n.-29-725C>A
ENST00000395048.6:c.-26-728C>A ENSP00000378488.2:n.-26-728C>A
ENST00000395049.8:c.-29-725C>A ENSP00000378489.4:n.-29-725C>A
ENST00000562201.5:c.-26-728C>A ENSP00000455340.1:n.-26-728C>A
ENST00000564596.5:c.-220-1317C>A ENSP00000457668.1:n.-220-1317C>A
ENST00000566503.1:c.-220-1317C>A ENSP00000455846.1:n.-220-1317C>A
ENST00000567032.5:c.-29-725C>A ENSP00000456585.1:n.-29-725C>A
ENST00000569630.5:c.-26-728C>A ENSP00000455051.1:n.-26-728C>A
ENST00000617691.4:c.-26-728C>A ENSP00000482863.1:n.-26-728C>A
NM_000499.3:c.-26-728C>A NP_000490.1:n.-26-728C>A
XM_005254185.1:c.-29-725C>A XP_005254242.1:n.-29-725C>A
NM_000499.5:c.-26-728C>A NP_000490.1:n.-26-728C>A
NM_001319216.2:c.-29-725C>A NP_001306145.1:n.-29-725C>A
NM_001319217.2:c.-29-725C>A MANE Select NP_001306146.1:n.-29-725C>A
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