Canonical Allele Identifier: CA491488300

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75013025A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720684A>T , CM000677.2:g.74720684A>T	GRCh38
NC_000015.9:g.75013025A>T , CM000677.1:g.75013025A>T	GRCh37
NC_000015.8:g.72800078A>T	NCBI36
NG_008431.1:g.3143A>T
NG_008431.2:g.3143A>T
NG_061374.1:g.9845T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1344T>A MANE Select	ENSP00000369050.3:p.Ile448=
ENST00000379727.7:c.1344T>A	ENSP00000369050.3:p.Ile448=
ENST00000395048.6:c.1344T>A	ENSP00000378488.2:p.Ile448=
ENST00000395049.8:c.1257T>A	ENSP00000378489.4:p.Ile419=
ENST00000567032.5:c.1344T>A	ENSP00000456585.1:p.Ile448=
ENST00000612821.4:c.1260T>A	ENSP00000479744.1:p.Ile420=
ENST00000617691.4:c.1257T>A	ENSP00000482863.1:p.Ile419=
NM_000499.3:c.1344T>A	NP_000490.1:p.Ile448=
XM_005254185.1:c.1344T>A	XP_005254242.1:p.Ile448=
NM_000499.5:c.1344T>A	NP_000490.1:p.Ile448=
NM_001319216.2:c.1257T>A	NP_001306145.1:p.Ile419=
NM_001319217.2:c.1344T>A MANE Select	NP_001306146.1:p.Ile448=