Canonical Allele Identifier: CA491488360

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720741-A-G
• MyVariant Identifiers: chr15:g.75013082A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720741A>G , CM000677.2:g.74720741A>G	GRCh38
NC_000015.9:g.75013082A>G , CM000677.1:g.75013082A>G	GRCh37
NC_000015.8:g.72800135A>G	NCBI36
NG_008431.1:g.3200A>G
NG_008431.2:g.3200A>G
NG_061374.1:g.9788T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1287T>C MANE Select	ENSP00000369050.3:p.Pro429=
ENST00000379727.7:c.1287T>C	ENSP00000369050.3:p.Pro429=
ENST00000395048.6:c.1287T>C	ENSP00000378488.2:p.Pro429=
ENST00000395049.8:c.1200T>C	ENSP00000378489.4:p.Pro400=
ENST00000562201.5:c.*524T>C	ENSP00000455340.1:n.*524T>C
ENST00000564596.5:c.*222T>C	ENSP00000457668.1:n.*222T>C
ENST00000566503.1:c.504T>C	ENSP00000455846.1:p.Pro168=
ENST00000567032.5:c.1287T>C	ENSP00000456585.1:p.Pro429=
ENST00000569630.5:c.*876T>C	ENSP00000455051.1:n.*876T>C
ENST00000612821.4:c.1203T>C	ENSP00000479744.1:p.Pro401=
ENST00000617691.4:c.1200T>C	ENSP00000482863.1:p.Pro400=
NM_000499.3:c.1287T>C	NP_000490.1:p.Pro429=
XM_005254185.1:c.1287T>C	XP_005254242.1:p.Pro429=
NM_000499.5:c.1287T>C	NP_000490.1:p.Pro429=
NM_001319216.2:c.1200T>C	NP_001306145.1:p.Pro400=
NM_001319217.2:c.1287T>C MANE Select	NP_001306146.1:p.Pro429=