Canonical Allele Identifier: CA2187814568

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719781_74719782delinsCT , CM000677.2:g.74719781_74719782delinsCT	GRCh38
NC_000015.9:g.75012122_75012123delinsCT , CM000677.1:g.75012122_75012123delinsCT	GRCh37
NC_000015.8:g.72799175_72799176delinsCT	NCBI36
NG_008431.1:g.2240_2241delinsCT
NG_008431.2:g.2240_2241delinsCT
NG_061374.1:g.10747_10748delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*707_*708delinsAG MANE Select	ENSP00000369050.3:n.*707_*708delinsAG
ENST00000379727.7:c.*707_*708delinsAG	ENSP00000369050.3:n.*707_*708delinsAG
ENST00000395048.6:c.*707_*708delinsAG	ENSP00000378488.2:n.*707_*708delinsAG
ENST00000612821.4:c.2162_2163delinsAG	ENSP00000479744.1:n.2162_2163delinsAG
ENST00000617691.4:c.*707_*708delinsAG	ENSP00000482863.1:n.*707_*708delinsAG
NM_000499.3:c.*707_*708delinsAG	NP_000490.1:n.*707_*708delinsAG
XM_005254185.1:c.*707_*708delinsAG	XP_005254242.1:n.*707_*708delinsAG
NM_000499.5:c.*707_*708delinsAG	NP_000490.1:n.*707_*708delinsAG
NM_001319216.2:c.*707_*708delinsAG	NP_001306145.1:n.*707_*708delinsAG
NM_001319217.2:c.*707_*708delinsAG MANE Select	NP_001306146.1:n.*707_*708delinsAG