Canonical Allele Identifier: CA2187814528

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719686_74719689delinsTAGA , CM000677.2:g.74719686_74719689delinsTAGA	GRCh38
NC_000015.9:g.75012027_75012030delinsTAGA , CM000677.1:g.75012027_75012030delinsTAGA	GRCh37
NC_000015.8:g.72799080_72799083delinsTAGA	NCBI36
NG_008431.1:g.2145_2148delinsTAGA
NG_008431.2:g.2145_2148delinsTAGA
NG_061374.1:g.10840_10843delinsTCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*800_*803delinsTCTA MANE Select	ENSP00000369050.3:n.*800_*803delinsTCTA
ENST00000379727.7:c.*800_*803delinsTCTA	ENSP00000369050.3:n.*800_*803delinsTCTA
ENST00000395048.6:c.*800_*803delinsTCTA	ENSP00000378488.2:n.*800_*803delinsTCTA
ENST00000612821.4:c.2255_2258delinsTCTA	ENSP00000479744.1:n.2255_2258delinsTCTA
ENST00000617691.4:c.*800_*803delinsTCTA	ENSP00000482863.1:n.*800_*803delinsTCTA
NM_000499.3:c.*800_*803delinsTCTA	NP_000490.1:n.*800_*803delinsTCTA
XM_005254185.1:c.*800_*803delinsTCTA	XP_005254242.1:n.*800_*803delinsTCTA
NM_000499.5:c.*800_*803delinsTCTA	NP_000490.1:n.*800_*803delinsTCTA
NM_001319216.2:c.*800_*803delinsTCTA	NP_001306145.1:n.*800_*803delinsTCTA
NM_001319217.2:c.*800_*803delinsTCTA MANE Select	NP_001306146.1:n.*800_*803delinsTCTA