Canonical Allele Identifier: CA393164466

Gene: CYP1A1

Linked Data

• MyVariant Identifiers: chr15:g.75013066G>T (hg19) ; chr15:g.74720725G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720725G>T , CM000677.2:g.74720725G>T	GRCh38
NC_000015.9:g.75013066G>T , CM000677.1:g.75013066G>T	GRCh37
NC_000015.8:g.72800119G>T	NCBI36
NG_008431.1:g.3184G>T
NG_008431.2:g.3184G>T
NG_061374.1:g.9804C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1303C>A MANE Select	ENSP00000369050.3:p.Pro435Thr
ENST00000379727.7:c.1303C>A	ENSP00000369050.3:p.Pro435Thr
ENST00000395048.6:c.1303C>A	ENSP00000378488.2:p.Pro435Thr
ENST00000395049.8:c.1216C>A	ENSP00000378489.4:p.Pro406Thr
ENST00000562201.5:c.*540C>A	ENSP00000455340.1:n.*540C>A
ENST00000564596.5:c.*238C>A	ENSP00000457668.1:n.*238C>A
ENST00000566503.1:c.520C>A	ENSP00000455846.1:p.Pro174Thr
ENST00000567032.5:c.1303C>A	ENSP00000456585.1:p.Pro435Thr
ENST00000569630.5:c.*892C>A	ENSP00000455051.1:n.*892C>A
ENST00000612821.4:c.1219C>A	ENSP00000479744.1:p.Pro407Thr
ENST00000617691.4:c.1216C>A	ENSP00000482863.1:p.Pro406Thr
NM_000499.3:c.1303C>A	NP_000490.1:p.Pro435Thr
XM_005254185.1:c.1303C>A	XP_005254242.1:p.Pro435Thr
NM_000499.5:c.1303C>A	NP_000490.1:p.Pro435Thr
NM_001319216.2:c.1216C>A	NP_001306145.1:p.Pro406Thr
NM_001319217.2:c.1303C>A MANE Select	NP_001306146.1:p.Pro435Thr