Canonical Allele Identifier: CA2629503381

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74719885-TAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719887_74719888del , CM000677.2:g.74719887_74719888del	GRCh38
NC_000015.9:g.75012228_75012229del , CM000677.1:g.75012228_75012229del	GRCh37
NC_000015.8:g.72799281_72799282del	NCBI36
NG_008431.1:g.2346_2347del
NG_008431.2:g.2346_2347del
NG_061374.1:g.10642_10643del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*602_*603del MANE Select	ENSP00000369050.3:n.*602_*603del
ENST00000379727.7:c.*602_*603del	ENSP00000369050.3:n.*602_*603del
ENST00000395048.6:c.*602_*603del	ENSP00000378488.2:n.*602_*603del
ENST00000612821.4:c.2057_2058del	ENSP00000479744.1:n.2057_2058del
ENST00000617691.4:c.*602_*603del	ENSP00000482863.1:n.*602_*603del
NM_000499.3:c.*602_*603del	NP_000490.1:n.*602_*603del
XM_005254185.1:c.*602_*603del	XP_005254242.1:n.*602_*603del
NM_000499.5:c.*602_*603del	NP_000490.1:n.*602_*603del
NM_001319216.2:c.*602_*603del	NP_001306145.1:n.*602_*603del
NM_001319217.2:c.*602_*603del MANE Select	NP_001306146.1:n.*602_*603del