Canonical Allele Identifier: CA393164487

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720731-G-C
• MyVariant Identifiers: chr15:g.75013072G>C (hg19) ; chr15:g.74720731G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720731G>C , CM000677.2:g.74720731G>C	GRCh38
NC_000015.9:g.75013072G>C , CM000677.1:g.75013072G>C	GRCh37
NC_000015.8:g.72800125G>C	NCBI36
NG_008431.1:g.3190G>C
NG_008431.2:g.3190G>C
NG_061374.1:g.9798C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1297C>G MANE Select	ENSP00000369050.3:p.Leu433Val
ENST00000379727.7:c.1297C>G	ENSP00000369050.3:p.Leu433Val
ENST00000395048.6:c.1297C>G	ENSP00000378488.2:p.Leu433Val
ENST00000395049.8:c.1210C>G	ENSP00000378489.4:p.Leu404Val
ENST00000562201.5:c.*534C>G	ENSP00000455340.1:n.*534C>G
ENST00000564596.5:c.*232C>G	ENSP00000457668.1:n.*232C>G
ENST00000566503.1:c.514C>G	ENSP00000455846.1:p.Leu172Val
ENST00000567032.5:c.1297C>G	ENSP00000456585.1:p.Leu433Val
ENST00000569630.5:c.*886C>G	ENSP00000455051.1:n.*886C>G
ENST00000612821.4:c.1213C>G	ENSP00000479744.1:p.Leu405Val
ENST00000617691.4:c.1210C>G	ENSP00000482863.1:p.Leu404Val
NM_000499.3:c.1297C>G	NP_000490.1:p.Leu433Val
XM_005254185.1:c.1297C>G	XP_005254242.1:p.Leu433Val
NM_000499.5:c.1297C>G	NP_000490.1:p.Leu433Val
NM_001319216.2:c.1210C>G	NP_001306145.1:p.Leu404Val
NM_001319217.2:c.1297C>G MANE Select	NP_001306146.1:p.Leu433Val