Canonical Allele Identifier: CA2187814929

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720636_74720637delinsGC , CM000677.2:g.74720636_74720637delinsGC	GRCh38
NC_000015.9:g.75012977_75012978delinsGC , CM000677.1:g.75012977_75012978delinsGC	GRCh37
NC_000015.8:g.72800030_72800031delinsGC	NCBI36
NG_008431.1:g.3095_3096delinsGC
NG_008431.2:g.3095_3096delinsGC
NG_061374.1:g.9892_9893delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1391_1392delinsGC MANE Select	ENSP00000369050.3:p.Arg464=
ENST00000379727.7:c.1391_1392delinsGC	ENSP00000369050.3:p.Arg464=
ENST00000395048.6:c.1391_1392delinsGC	ENSP00000378488.2:p.Arg464=
ENST00000395049.8:c.1304_1305delinsGC	ENSP00000378489.4:p.Arg435=
ENST00000567032.5:c.1391_1392delinsGC	ENSP00000456585.1:p.Arg464=
ENST00000612821.4:c.1307_1308delinsGC	ENSP00000479744.1:p.Arg436=
ENST00000617691.4:c.1304_1305delinsGC	ENSP00000482863.1:p.Arg435=
NM_000499.3:c.1391_1392delinsGC	NP_000490.1:p.Arg464=
XM_005254185.1:c.1391_1392delinsGC	XP_005254242.1:p.Arg464=
NM_000499.5:c.1391_1392delinsGC	NP_000490.1:p.Arg464=
NM_001319216.2:c.1304_1305delinsGC	NP_001306145.1:p.Arg435=
NM_001319217.2:c.1391_1392delinsGC MANE Select	NP_001306146.1:p.Arg464=