Canonical Allele Identifier: CA2187814925

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74720626_74720633delinsAGACCTCC , CM000677.2:g.74720626_74720633delinsAGACCTCC	GRCh38
NC_000015.9:g.75012967_75012974delinsAGACCTCC , CM000677.1:g.75012967_75012974delinsAGACCTCC	GRCh37
NC_000015.8:g.72800020_72800027delinsAGACCTCC	NCBI36
NG_008431.1:g.3085_3092delinsAGACCTCC
NG_008431.2:g.3085_3092delinsAGACCTCC
NG_061374.1:g.9896_9903delinsGGAGGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.1395_1402delinsGGAGGTCT MANE Select	ENSP00000369050.3:p.Trp465=
ENST00000379727.7:c.1395_1402delinsGGAGGTCT	ENSP00000369050.3:p.Trp465=
ENST00000395048.6:c.1395_1402delinsGGAGGTCT	ENSP00000378488.2:p.Trp465=
ENST00000395049.8:c.1308_1315delinsGGAGGTCT	ENSP00000378489.4:p.Trp436=
ENST00000567032.5:c.1395_1402delinsGGAGGTCT	ENSP00000456585.1:p.Trp465=
ENST00000612821.4:c.1311_1318delinsGGAGGTCT	ENSP00000479744.1:p.Trp437=
ENST00000617691.4:c.1308_1315delinsGGAGGTCT	ENSP00000482863.1:p.Trp436=
NM_000499.3:c.1395_1402delinsGGAGGTCT	NP_000490.1:p.Trp465=
XM_005254185.1:c.1395_1402delinsGGAGGTCT	XP_005254242.1:p.Trp465=
NM_000499.5:c.1395_1402delinsGGAGGTCT	NP_000490.1:p.Trp465=
NM_001319216.2:c.1308_1315delinsGGAGGTCT	NP_001306145.1:p.Trp436=
NM_001319217.2:c.1395_1402delinsGGAGGTCT MANE Select	NP_001306146.1:p.Trp465=