Canonical Allele Identifier: CA2629506349

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720705-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720707dup , CM000677.2:g.74720707dup	GRCh38
NC_000015.9:g.75013048dup , CM000677.1:g.75013048dup	GRCh37
NC_000015.8:g.72800101dup	NCBI36
NG_008431.1:g.3166dup
NG_008431.2:g.3166dup
NG_061374.1:g.9823dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1322dup MANE Select	ENSP00000369050.3:p.Val442GlyfsTer4
ENST00000379727.7:c.1322dup	ENSP00000369050.3:p.Val442GlyfsTer4
ENST00000395048.6:c.1322dup	ENSP00000378488.2:p.Val442GlyfsTer4
ENST00000395049.8:c.1235dup	ENSP00000378489.4:p.Val413GlyfsTer4
ENST00000567032.5:c.1322dup	ENSP00000456585.1:p.Val442GlyfsTer4
ENST00000612821.4:c.1238dup	ENSP00000479744.1:p.Val414GlyfsTer4
ENST00000617691.4:c.1235dup	ENSP00000482863.1:p.Val413GlyfsTer4
NM_000499.3:c.1322dup	NP_000490.1:p.Val442GlyfsTer4
XM_005254185.1:c.1322dup	XP_005254242.1:p.Val442GlyfsTer4
NM_000499.5:c.1322dup	NP_000490.1:p.Val442GlyfsTer4
NM_001319216.2:c.1235dup	NP_001306145.1:p.Val413GlyfsTer4
NM_001319217.2:c.1322dup MANE Select	NP_001306146.1:p.Val442GlyfsTer4