Canonical Allele Identifier: CA2187814908

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720598_74720600delinsCGT , CM000677.2:g.74720598_74720600delinsCGT	GRCh38
NC_000015.9:g.75012939_75012941delinsCGT , CM000677.1:g.75012939_75012941delinsCGT	GRCh37
NC_000015.8:g.72799992_72799994delinsCGT	NCBI36
NG_008431.1:g.3057_3059delinsCGT
NG_008431.2:g.3057_3059delinsCGT
NG_061374.1:g.9929_9931delinsACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1428_1430delinsACG MANE Select	ENSP00000369050.3:p.Gln476=
ENST00000379727.7:c.1428_1430delinsACG	ENSP00000369050.3:p.Gln476=
ENST00000395048.6:c.1428_1430delinsACG	ENSP00000378488.2:p.Gln476=
ENST00000395049.8:c.1341_1343delinsACG	ENSP00000378489.4:p.Gln447=
ENST00000567032.5:c.1428_1430delinsACG	ENSP00000456585.1:p.Gln476=
ENST00000612821.4:c.1344_1346delinsACG	ENSP00000479744.1:p.Gln448=
ENST00000617691.4:c.1341_1343delinsACG	ENSP00000482863.1:p.Gln447=
NM_000499.3:c.1428_1430delinsACG	NP_000490.1:p.Gln476=
XM_005254185.1:c.1428_1430delinsACG	XP_005254242.1:p.Gln476=
NM_000499.5:c.1428_1430delinsACG	NP_000490.1:p.Gln476=
NM_001319216.2:c.1341_1343delinsACG	NP_001306145.1:p.Gln447=
NM_001319217.2:c.1428_1430delinsACG MANE Select	NP_001306146.1:p.Gln476=