Canonical Allele Identifier: CA2187814970

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720722_74720723delinsCA , CM000677.2:g.74720722_74720723delinsCA	GRCh38
NC_000015.9:g.75013063_75013064delinsCA , CM000677.1:g.75013063_75013064delinsCA	GRCh37
NC_000015.8:g.72800116_72800117delinsCA	NCBI36
NG_008431.1:g.3181_3182delinsCA
NG_008431.2:g.3181_3182delinsCA
NG_061374.1:g.9806_9807delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1305_1306delinsTG MANE Select	ENSP00000369050.3:p.Pro435=
ENST00000379727.7:c.1305_1306delinsTG	ENSP00000369050.3:p.Pro435=
ENST00000395048.6:c.1305_1306delinsTG	ENSP00000378488.2:p.Pro435=
ENST00000395049.8:c.1218_1219delinsTG	ENSP00000378489.4:p.Pro406=
ENST00000562201.5:c.*542_*543delinsTG	ENSP00000455340.1:n.*542_*543delinsTG
ENST00000564596.5:c.*240_*241delinsTG	ENSP00000457668.1:n.*240_*241delinsTG
ENST00000566503.1:c.522_523delinsTG	ENSP00000455846.1:p.Pro174=
ENST00000567032.5:c.1305_1306delinsTG	ENSP00000456585.1:p.Pro435=
ENST00000569630.5:c.*894_*895delinsTG	ENSP00000455051.1:n.*894_*895delinsTG
ENST00000612821.4:c.1221_1222delinsTG	ENSP00000479744.1:p.Pro407=
ENST00000617691.4:c.1218_1219delinsTG	ENSP00000482863.1:p.Pro406=
NM_000499.3:c.1305_1306delinsTG	NP_000490.1:p.Pro435=
XM_005254185.1:c.1305_1306delinsTG	XP_005254242.1:p.Pro435=
NM_000499.5:c.1305_1306delinsTG	NP_000490.1:p.Pro435=
NM_001319216.2:c.1218_1219delinsTG	NP_001306145.1:p.Pro406=
NM_001319217.2:c.1305_1306delinsTG MANE Select	NP_001306146.1:p.Pro435=