Canonical Allele Identifier: CA2629506097

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720616-AG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720618del , CM000677.2:g.74720618del	GRCh38
NC_000015.9:g.75012959del , CM000677.1:g.75012959del	GRCh37
NC_000015.8:g.72800012del	NCBI36
NG_008431.1:g.3077del
NG_008431.2:g.3077del
NG_061374.1:g.9912del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1411del MANE Select	ENSP00000369050.3:p.Leu471TrpfsTer16
ENST00000379727.7:c.1411del	ENSP00000369050.3:p.Leu471TrpfsTer16
ENST00000395048.6:c.1411del	ENSP00000378488.2:p.Leu471TrpfsTer16
ENST00000395049.8:c.1324del	ENSP00000378489.4:p.Leu442TrpfsTer16
ENST00000567032.5:c.1411del	ENSP00000456585.1:p.Leu471TrpfsTer16
ENST00000612821.4:c.1327del	ENSP00000479744.1:p.Leu443TrpfsTer16
ENST00000617691.4:c.1324del	ENSP00000482863.1:p.Leu442TrpfsTer16
NM_000499.3:c.1411del	NP_000490.1:p.Leu471TrpfsTer16
XM_005254185.1:c.1411del	XP_005254242.1:p.Leu471TrpfsTer16
NM_000499.5:c.1411del	NP_000490.1:p.Leu471TrpfsTer16
NM_001319216.2:c.1324del	NP_001306145.1:p.Leu442TrpfsTer16
NM_001319217.2:c.1411del MANE Select	NP_001306146.1:p.Leu471TrpfsTer16