Canonical Allele Identifier: CA971510001

Gene: CYP1A1

Linked Data

• dbSNP Id: rs2063152892
• gnomAD v3: 15-74719673-ATGCAGGCTAGAATAGAAGGATTGT-A
• gnomAD v4: 15-74719673-ATGCAGGCTAGAATAGAAGGATTGT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719676_74719699del , CM000677.2:g.74719676_74719699del	GRCh38
NC_000015.9:g.75012017_75012040del , CM000677.1:g.75012017_75012040del	GRCh37
NC_000015.8:g.72799070_72799093del	NCBI36
NG_008431.1:g.2135_2158del
NG_008431.2:g.2135_2158del
NG_061374.1:g.10832_10855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*792_*815del MANE Select	ENSP00000369050.3:n.*792_*815del
ENST00000379727.7:c.*792_*815del	ENSP00000369050.3:n.*792_*815del
ENST00000395048.6:c.*792_*815del	ENSP00000378488.2:n.*792_*815del
ENST00000612821.4:c.2247_2270del	ENSP00000479744.1:n.2247_2270del
ENST00000617691.4:c.*792_*815del	ENSP00000482863.1:n.*792_*815del
NM_000499.3:c.*792_*815del	NP_000490.1:n.*792_*815del
XM_005254185.1:c.*792_*815del	XP_005254242.1:n.*792_*815del
NM_000499.5:c.*792_*815del	NP_000490.1:n.*792_*815del
NM_001319216.2:c.*792_*815del	NP_001306145.1:n.*792_*815del
NM_001319217.2:c.*792_*815del MANE Select	NP_001306146.1:n.*792_*815del