Canonical Allele Identifier: CA2629506452

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720792-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720792C>T , CM000677.2:g.74720792C>T	GRCh38
NC_000015.9:g.75013133C>T , CM000677.1:g.75013133C>T	GRCh37
NC_000015.8:g.72800186C>T	NCBI36
NG_008431.1:g.3251C>T
NG_008431.2:g.3251C>T
NG_061374.1:g.9737G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1254-18G>A MANE Select	ENSP00000369050.3:n.1254-18G>A
ENST00000379727.7:c.1254-18G>A	ENSP00000369050.3:n.1254-18G>A
ENST00000395048.6:c.1254-18G>A	ENSP00000378488.2:n.1254-18G>A
ENST00000395049.8:c.1167-18G>A	ENSP00000378489.4:n.1167-18G>A
ENST00000562201.5:c.*491-18G>A	ENSP00000455340.1:n.*491-18G>A
ENST00000564596.5:c.*171G>A	ENSP00000457668.1:n.*171G>A
ENST00000566503.1:c.471-18G>A	ENSP00000455846.1:n.471-18G>A
ENST00000567032.5:c.1254-18G>A	ENSP00000456585.1:n.1254-18G>A
ENST00000569630.5:c.*843-18G>A	ENSP00000455051.1:n.*843-18G>A
ENST00000612821.4:c.1170-18G>A	ENSP00000479744.1:n.1170-18G>A
ENST00000617691.4:c.1167-18G>A	ENSP00000482863.1:n.1167-18G>A
NM_000499.3:c.1254-18G>A	NP_000490.1:n.1254-18G>A
XM_005254185.1:c.1254-18G>A	XP_005254242.1:n.1254-18G>A
NM_000499.5:c.1254-18G>A	NP_000490.1:n.1254-18G>A
NM_001319216.2:c.1167-18G>A	NP_001306145.1:n.1167-18G>A
NM_001319217.2:c.1254-18G>A MANE Select	NP_001306146.1:n.1254-18G>A