Canonical Allele Identifier: CA2629506127

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720629-CCTCCCAGCGGGCAAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720630_74720644del , CM000677.2:g.74720630_74720644del	GRCh38
NC_000015.9:g.75012971_75012985del , CM000677.1:g.75012971_75012985del	GRCh37
NC_000015.8:g.72800024_72800038del	NCBI36
NG_008431.1:g.3089_3103del
NG_008431.2:g.3089_3103del
NG_061374.1:g.9885_9899del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1384_1398del MANE Select	ENSP00000369050.3:p.Ile462_Glu466del
ENST00000379727.7:c.1384_1398del	ENSP00000369050.3:p.Ile462_Glu466del
ENST00000395048.6:c.1384_1398del	ENSP00000378488.2:p.Ile462_Glu466del
ENST00000395049.8:c.1297_1311del	ENSP00000378489.4:p.Ile433_Glu437del
ENST00000567032.5:c.1384_1398del	ENSP00000456585.1:p.Ile462_Glu466del
ENST00000612821.4:c.1300_1314del	ENSP00000479744.1:p.Ile434_Glu438del
ENST00000617691.4:c.1297_1311del	ENSP00000482863.1:p.Ile433_Glu437del
NM_000499.3:c.1384_1398del	NP_000490.1:p.Ile462_Glu466del
XM_005254185.1:c.1384_1398del	XP_005254242.1:p.Ile462_Glu466del
NM_000499.5:c.1384_1398del	NP_000490.1:p.Ile462_Glu466del
NM_001319216.2:c.1297_1311del	NP_001306145.1:p.Ile433_Glu437del
NM_001319217.2:c.1384_1398del MANE Select	NP_001306146.1:p.Ile462_Glu466del