Canonical Allele Identifier: CA491488354

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720737-G-T
• MyVariant Identifiers: chr15:g.75013078G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720737G>T , CM000677.2:g.74720737G>T	GRCh38
NC_000015.9:g.75013078G>T , CM000677.1:g.75013078G>T	GRCh37
NC_000015.8:g.72800131G>T	NCBI36
NG_008431.1:g.3196G>T
NG_008431.2:g.3196G>T
NG_061374.1:g.9792C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1291C>A MANE Select	ENSP00000369050.3:p.Arg431=
ENST00000379727.7:c.1291C>A	ENSP00000369050.3:p.Arg431=
ENST00000395048.6:c.1291C>A	ENSP00000378488.2:p.Arg431=
ENST00000395049.8:c.1204C>A	ENSP00000378489.4:p.Arg402=
ENST00000562201.5:c.*528C>A	ENSP00000455340.1:n.*528C>A
ENST00000564596.5:c.*226C>A	ENSP00000457668.1:n.*226C>A
ENST00000566503.1:c.508C>A	ENSP00000455846.1:p.Arg170=
ENST00000567032.5:c.1291C>A	ENSP00000456585.1:p.Arg431=
ENST00000569630.5:c.*880C>A	ENSP00000455051.1:n.*880C>A
ENST00000612821.4:c.1207C>A	ENSP00000479744.1:p.Arg403=
ENST00000617691.4:c.1204C>A	ENSP00000482863.1:p.Arg402=
NM_000499.3:c.1291C>A	NP_000490.1:p.Arg431=
XM_005254185.1:c.1291C>A	XP_005254242.1:p.Arg431=
NM_000499.5:c.1291C>A	NP_000490.1:p.Arg431=
NM_001319216.2:c.1204C>A	NP_001306145.1:p.Arg402=
NM_001319217.2:c.1291C>A MANE Select	NP_001306146.1:p.Arg431=