Canonical Allele Identifier: CA393164477

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75013069T>C (hg19) ; chr15:g.74720728T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720728T>C , CM000677.2:g.74720728T>C	GRCh38
NC_000015.9:g.75013069T>C , CM000677.1:g.75013069T>C	GRCh37
NC_000015.8:g.72800122T>C	NCBI36
NG_008431.1:g.3187T>C
NG_008431.2:g.3187T>C
NG_061374.1:g.9801A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1300A>G MANE Select	ENSP00000369050.3:p.Thr434Ala
ENST00000379727.7:c.1300A>G	ENSP00000369050.3:p.Thr434Ala
ENST00000395048.6:c.1300A>G	ENSP00000378488.2:p.Thr434Ala
ENST00000395049.8:c.1213A>G	ENSP00000378489.4:p.Thr405Ala
ENST00000562201.5:c.*537A>G	ENSP00000455340.1:n.*537A>G
ENST00000564596.5:c.*235A>G	ENSP00000457668.1:n.*235A>G
ENST00000566503.1:c.517A>G	ENSP00000455846.1:p.Thr173Ala
ENST00000567032.5:c.1300A>G	ENSP00000456585.1:p.Thr434Ala
ENST00000569630.5:c.*889A>G	ENSP00000455051.1:n.*889A>G
ENST00000612821.4:c.1216A>G	ENSP00000479744.1:p.Thr406Ala
ENST00000617691.4:c.1213A>G	ENSP00000482863.1:p.Thr405Ala
NM_000499.3:c.1300A>G	NP_000490.1:p.Thr434Ala
XM_005254185.1:c.1300A>G	XP_005254242.1:p.Thr434Ala
NM_000499.5:c.1300A>G	NP_000490.1:p.Thr434Ala
NM_001319216.2:c.1213A>G	NP_001306145.1:p.Thr405Ala
NM_001319217.2:c.1300A>G MANE Select	NP_001306146.1:p.Thr434Ala