Canonical Allele Identifier: CA2187814559

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719773_74719774delinsAC , CM000677.2:g.74719773_74719774delinsAC	GRCh38
NC_000015.9:g.75012114_75012115delinsAC , CM000677.1:g.75012114_75012115delinsAC	GRCh37
NC_000015.8:g.72799167_72799168delinsAC	NCBI36
NG_008431.1:g.2232_2233delinsAC
NG_008431.2:g.2232_2233delinsAC
NG_061374.1:g.10755_10756delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*715_*716delinsGT MANE Select	ENSP00000369050.3:n.*715_*716delinsGT
ENST00000379727.7:c.*715_*716delinsGT	ENSP00000369050.3:n.*715_*716delinsGT
ENST00000395048.6:c.*715_*716delinsGT	ENSP00000378488.2:n.*715_*716delinsGT
ENST00000612821.4:c.2170_2171delinsGT	ENSP00000479744.1:n.2170_2171delinsGT
ENST00000617691.4:c.*715_*716delinsGT	ENSP00000482863.1:n.*715_*716delinsGT
NM_000499.3:c.*715_*716delinsGT	NP_000490.1:n.*715_*716delinsGT
XM_005254185.1:c.*715_*716delinsGT	XP_005254242.1:n.*715_*716delinsGT
NM_000499.5:c.*715_*716delinsGT	NP_000490.1:n.*715_*716delinsGT
NM_001319216.2:c.*715_*716delinsGT	NP_001306145.1:n.*715_*716delinsGT
NM_001319217.2:c.*715_*716delinsGT MANE Select	NP_001306146.1:n.*715_*716delinsGT