Canonical Allele Identifier: CA2629505744

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720440-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720440C>A , CM000677.2:g.74720440C>A	GRCh38
NC_000015.9:g.75012781C>A , CM000677.1:g.75012781C>A	GRCh37
NC_000015.8:g.72799834C>A	NCBI36
NG_008431.1:g.2899C>A
NG_008431.2:g.2899C>A
NG_061374.1:g.10089G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*49G>T MANE Select	ENSP00000369050.3:n.*49G>T
ENST00000379727.7:c.*49G>T	ENSP00000369050.3:n.*49G>T
ENST00000395048.6:c.*49G>T	ENSP00000378488.2:n.*49G>T
ENST00000395049.8:c.*49G>T	ENSP00000378489.4:n.*49G>T
ENST00000567032.5:c.*49G>T	ENSP00000456585.1:n.*49G>T
ENST00000612821.4:c.1504G>T	ENSP00000479744.1:n.1504G>T
ENST00000617691.4:c.*49G>T	ENSP00000482863.1:n.*49G>T
NM_000499.3:c.*49G>T	NP_000490.1:n.*49G>T
XM_005254185.1:c.*49G>T	XP_005254242.1:n.*49G>T
NM_000499.5:c.*49G>T	NP_000490.1:n.*49G>T
NM_001319216.2:c.*49G>T	NP_001306145.1:n.*49G>T
NM_001319217.2:c.*49G>T MANE Select	NP_001306146.1:n.*49G>T