Canonical Allele Identifier: CA2629506367

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720710-C-CGAT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720711_74720713dup , CM000677.2:g.74720711_74720713dup	GRCh38
NC_000015.9:g.75013052_75013054dup , CM000677.1:g.75013052_75013054dup	GRCh37
NC_000015.8:g.72800105_72800107dup	NCBI36
NG_008431.1:g.3170_3172dup
NG_008431.2:g.3170_3172dup
NG_061374.1:g.9816_9818dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1315_1317dup MANE Select	ENSP00000369050.3:p.Ile439_Asp440insIle
ENST00000379727.7:c.1315_1317dup	ENSP00000369050.3:p.Ile439_Asp440insIle
ENST00000395048.6:c.1315_1317dup	ENSP00000378488.2:p.Ile439_Asp440insIle
ENST00000395049.8:c.1228_1230dup	ENSP00000378489.4:p.Ile410_Asp411insIle
ENST00000567032.5:c.1315_1317dup	ENSP00000456585.1:p.Ile439_Asp440insIle
ENST00000612821.4:c.1231_1233dup	ENSP00000479744.1:p.Ile411_Asp412insIle
ENST00000617691.4:c.1228_1230dup	ENSP00000482863.1:p.Ile410_Asp411insIle
NM_000499.3:c.1315_1317dup	NP_000490.1:p.Ile439_Asp440insIle
XM_005254185.1:c.1315_1317dup	XP_005254242.1:p.Ile439_Asp440insIle
NM_000499.5:c.1315_1317dup	NP_000490.1:p.Ile439_Asp440insIle
NM_001319216.2:c.1228_1230dup	NP_001306145.1:p.Ile410_Asp411insIle
NM_001319217.2:c.1315_1317dup MANE Select	NP_001306146.1:p.Ile439_Asp440insIle