Canonical Allele Identifier: CA2629505764

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720455-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720455T>C , CM000677.2:g.74720455T>C	GRCh38
NC_000015.9:g.75012796T>C , CM000677.1:g.75012796T>C	GRCh37
NC_000015.8:g.72799849T>C	NCBI36
NG_008431.1:g.2914T>C
NG_008431.2:g.2914T>C
NG_061374.1:g.10074A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*34A>G MANE Select	ENSP00000369050.3:n.*34A>G
ENST00000379727.7:c.*34A>G	ENSP00000369050.3:n.*34A>G
ENST00000395048.6:c.*34A>G	ENSP00000378488.2:n.*34A>G
ENST00000395049.8:c.*34A>G	ENSP00000378489.4:n.*34A>G
ENST00000567032.5:c.*34A>G	ENSP00000456585.1:n.*34A>G
ENST00000612821.4:c.1489A>G	ENSP00000479744.1:n.1489A>G
ENST00000617691.4:c.*34A>G	ENSP00000482863.1:n.*34A>G
NM_000499.3:c.*34A>G	NP_000490.1:n.*34A>G
XM_005254185.1:c.*34A>G	XP_005254242.1:n.*34A>G
NM_000499.5:c.*34A>G	NP_000490.1:n.*34A>G
NM_001319216.2:c.*34A>G	NP_001306145.1:n.*34A>G
NM_001319217.2:c.*34A>G MANE Select	NP_001306146.1:n.*34A>G