Canonical Allele Identifier: CA715665136

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1352611997
• MyVariant Identifiers: chr15:g.75011901_75011904del (hg19) ; chr15:g.74719560_74719563del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719561_74719564del , CM000677.2:g.74719561_74719564del	GRCh38
NC_000015.9:g.75011902_75011905del , CM000677.1:g.75011902_75011905del	GRCh37
NC_000015.8:g.72798955_72798958del	NCBI36
NG_008431.1:g.2020_2023del
NG_008431.2:g.2020_2023del
NG_061374.1:g.10966_10969del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*926_*929del MANE Select	ENSP00000369050.3:n.*926_*929del
ENST00000379727.7:c.*926_*929del	ENSP00000369050.3:n.*926_*929del
ENST00000395048.6:c.*926_*929del	ENSP00000378488.2:n.*926_*929del
ENST00000612821.4:c.2381_2384del	ENSP00000479744.1:n.2381_2384del
ENST00000617691.4:c.*926_*929del	ENSP00000482863.1:n.*926_*929del
NM_000499.3:c.*926_*929del	NP_000490.1:n.*926_*929del
XM_005254185.1:c.*926_*929del	XP_005254242.1:n.*926_*929del
NM_000499.5:c.*926_*929del	NP_000490.1:n.*926_*929del
NM_001319216.2:c.*926_*929del	NP_001306145.1:n.*926_*929del
NM_001319217.2:c.*926_*929del MANE Select	NP_001306146.1:n.*926_*929del