Canonical Allele Identifier: CA2629505758

Gene: CYP1A1

Linked Data

• gnomAD v4: 15-74720453-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720453G>C , CM000677.2:g.74720453G>C	GRCh38
NC_000015.9:g.75012794G>C , CM000677.1:g.75012794G>C	GRCh37
NC_000015.8:g.72799847G>C	NCBI36
NG_008431.1:g.2912G>C
NG_008431.2:g.2912G>C
NG_061374.1:g.10076C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*36C>G MANE Select	ENSP00000369050.3:n.*36C>G
ENST00000379727.7:c.*36C>G	ENSP00000369050.3:n.*36C>G
ENST00000395048.6:c.*36C>G	ENSP00000378488.2:n.*36C>G
ENST00000395049.8:c.*36C>G	ENSP00000378489.4:n.*36C>G
ENST00000567032.5:c.*36C>G	ENSP00000456585.1:n.*36C>G
ENST00000612821.4:c.1491C>G	ENSP00000479744.1:n.1491C>G
ENST00000617691.4:c.*36C>G	ENSP00000482863.1:n.*36C>G
NM_000499.3:c.*36C>G	NP_000490.1:n.*36C>G
XM_005254185.1:c.*36C>G	XP_005254242.1:n.*36C>G
NM_000499.5:c.*36C>G	NP_000490.1:n.*36C>G
NM_001319216.2:c.*36C>G	NP_001306145.1:n.*36C>G
NM_001319217.2:c.*36C>G MANE Select	NP_001306146.1:n.*36C>G