Canonical Allele Identifier: CA393164513

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75013079T>A (hg19) ; chr15:g.74720738T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720738T>A , CM000677.2:g.74720738T>A	GRCh38
NC_000015.9:g.75013079T>A , CM000677.1:g.75013079T>A	GRCh37
NC_000015.8:g.72800132T>A	NCBI36
NG_008431.1:g.3197T>A
NG_008431.2:g.3197T>A
NG_061374.1:g.9791A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1290A>T MANE Select	ENSP00000369050.3:p.Glu430Asp
ENST00000379727.7:c.1290A>T	ENSP00000369050.3:p.Glu430Asp
ENST00000395048.6:c.1290A>T	ENSP00000378488.2:p.Glu430Asp
ENST00000395049.8:c.1203A>T	ENSP00000378489.4:p.Glu401Asp
ENST00000562201.5:c.*527A>T	ENSP00000455340.1:n.*527A>T
ENST00000564596.5:c.*225A>T	ENSP00000457668.1:n.*225A>T
ENST00000566503.1:c.507A>T	ENSP00000455846.1:p.Glu169Asp
ENST00000567032.5:c.1290A>T	ENSP00000456585.1:p.Glu430Asp
ENST00000569630.5:c.*879A>T	ENSP00000455051.1:n.*879A>T
ENST00000612821.4:c.1206A>T	ENSP00000479744.1:p.Glu402Asp
ENST00000617691.4:c.1203A>T	ENSP00000482863.1:p.Glu401Asp
NM_000499.3:c.1290A>T	NP_000490.1:p.Glu430Asp
XM_005254185.1:c.1290A>T	XP_005254242.1:p.Glu430Asp
NM_000499.5:c.1290A>T	NP_000490.1:p.Glu430Asp
NM_001319216.2:c.1203A>T	NP_001306145.1:p.Glu401Asp
NM_001319217.2:c.1290A>T MANE Select	NP_001306146.1:p.Glu430Asp