Canonical Allele Identifier: CA491488262

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75012992A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720651A>G , CM000677.2:g.74720651A>G	GRCh38
NC_000015.9:g.75012992A>G , CM000677.1:g.75012992A>G	GRCh37
NC_000015.8:g.72800045A>G	NCBI36
NG_008431.1:g.3110A>G
NG_008431.2:g.3110A>G
NG_061374.1:g.9878T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000379727.8:c.1377T>C MANE Select	ENSP00000369050.3:p.Gly459=
ENST00000379727.7:c.1377T>C	ENSP00000369050.3:p.Gly459=
ENST00000395048.6:c.1377T>C	ENSP00000378488.2:p.Gly459=
ENST00000395049.8:c.1290T>C	ENSP00000378489.4:p.Gly430=
ENST00000567032.5:c.1377T>C	ENSP00000456585.1:p.Gly459=
ENST00000612821.4:c.1293T>C	ENSP00000479744.1:p.Gly431=
ENST00000617691.4:c.1290T>C	ENSP00000482863.1:p.Gly430=
NM_000499.3:c.1377T>C	NP_000490.1:p.Gly459=
XM_005254185.1:c.1377T>C	XP_005254242.1:p.Gly459=
NM_000499.5:c.1377T>C	NP_000490.1:p.Gly459=
NM_001319216.2:c.1290T>C	NP_001306145.1:p.Gly430=
NM_001319217.2:c.1377T>C MANE Select	NP_001306146.1:p.Gly459=