Canonical Allele Identifier: CA715665475

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1352499352
• gnomAD v3: 15-74720636-GC-G
• gnomAD v4: 15-74720636-GC-G
• MyVariant Identifiers: chr15:g.75012978del (hg19) ; chr15:g.74720637del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720637del , CM000677.2:g.74720637del	GRCh38
NC_000015.9:g.75012978del , CM000677.1:g.75012978del	GRCh37
NC_000015.8:g.72800031del	NCBI36
NG_008431.1:g.3096del
NG_008431.2:g.3096del
NG_061374.1:g.9892del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1391del MANE Select	ENSP00000369050.3:p.Arg464ProfsTer23
ENST00000379727.7:c.1391del	ENSP00000369050.3:p.Arg464ProfsTer23
ENST00000395048.6:c.1391del	ENSP00000378488.2:p.Arg464ProfsTer23
ENST00000395049.8:c.1304del	ENSP00000378489.4:p.Arg435ProfsTer23
ENST00000567032.5:c.1391del	ENSP00000456585.1:p.Arg464ProfsTer23
ENST00000612821.4:c.1307del	ENSP00000479744.1:p.Arg436ProfsTer23
ENST00000617691.4:c.1304del	ENSP00000482863.1:p.Arg435ProfsTer23
NM_000499.3:c.1391del	NP_000490.1:p.Arg464ProfsTer23
XM_005254185.1:c.1391del	XP_005254242.1:p.Arg464ProfsTer23
NM_000499.5:c.1391del	NP_000490.1:p.Arg464ProfsTer23
NM_001319216.2:c.1304del	NP_001306145.1:p.Arg435ProfsTer23
NM_001319217.2:c.1391del MANE Select	NP_001306146.1:p.Arg464ProfsTer23