Canonical Allele Identifier: CA619412606

Gene: CYP1A1

Linked Data

• dbSNP Id: rs1166888365
• gnomAD v2: 15-75012998-A-ACACTTCC
• gnomAD v3: 15-74720657-A-ACACTTCC
• gnomAD v4: 15-74720657-A-ACACTTCC
• COSMIC: COSM1683683
• MyVariant Identifiers: chr15:g.75012998_75012999insCACTTCC (hg19) ; chr15:g.74720657_74720658insCACTTCC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720658_74720664dup , CM000677.2:g.74720658_74720664dup	GRCh38
NC_000015.9:g.75012999_75013005dup , CM000677.1:g.75012999_75013005dup	GRCh37
NC_000015.8:g.72800052_72800058dup	NCBI36
NG_008431.1:g.3117_3123dup
NG_008431.2:g.3117_3123dup
NG_061374.1:g.9865_9871dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1364_1370dup MANE Select	ENSP00000369050.3:p.Cys457TrpfsTer6
ENST00000379727.7:c.1364_1370dup	ENSP00000369050.3:p.Cys457TrpfsTer6
ENST00000395048.6:c.1364_1370dup	ENSP00000378488.2:p.Cys457TrpfsTer6
ENST00000395049.8:c.1277_1283dup	ENSP00000378489.4:p.Cys428TrpfsTer6
ENST00000567032.5:c.1364_1370dup	ENSP00000456585.1:p.Cys457TrpfsTer6
ENST00000612821.4:c.1280_1286dup	ENSP00000479744.1:p.Cys429TrpfsTer6
ENST00000617691.4:c.1277_1283dup	ENSP00000482863.1:p.Cys428TrpfsTer6
NM_000499.3:c.1364_1370dup	NP_000490.1:p.Cys457TrpfsTer6
XM_005254185.1:c.1364_1370dup	XP_005254242.1:p.Cys457TrpfsTer6
NM_000499.5:c.1364_1370dup	NP_000490.1:p.Cys457TrpfsTer6
NM_001319216.2:c.1277_1283dup	NP_001306145.1:p.Cys428TrpfsTer6
NM_001319217.2:c.1364_1370dup MANE Select	NP_001306146.1:p.Cys457TrpfsTer6