Canonical Allele Identifier: CA2629502917

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74719773-A-ACCC

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719779_74719781dup , CM000677.2:g.74719779_74719781dup	GRCh38
NC_000015.9:g.75012120_75012122dup , CM000677.1:g.75012120_75012122dup	GRCh37
NC_000015.8:g.72799173_72799175dup	NCBI36
NG_008431.1:g.2238_2240dup
NG_008431.2:g.2238_2240dup
NG_061374.1:g.10753_10755dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*713_*715dup MANE Select	ENSP00000369050.3:n.*713_*715dup
ENST00000379727.7:c.*713_*715dup	ENSP00000369050.3:n.*713_*715dup
ENST00000395048.6:c.*713_*715dup	ENSP00000378488.2:n.*713_*715dup
ENST00000612821.4:c.2168_2170dup	ENSP00000479744.1:n.2168_2170dup
ENST00000617691.4:c.*713_*715dup	ENSP00000482863.1:n.*713_*715dup
NM_000499.3:c.*713_*715dup	NP_000490.1:n.*713_*715dup
XM_005254185.1:c.*713_*715dup	XP_005254242.1:n.*713_*715dup
NM_000499.5:c.*713_*715dup	NP_000490.1:n.*713_*715dup
NM_001319216.2:c.*713_*715dup	NP_001306145.1:n.*713_*715dup
NM_001319217.2:c.*713_*715dup MANE Select	NP_001306146.1:n.*713_*715dup