Canonical Allele Identifier: CA2546629806

Gene: CYP1A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.74719750_74719751insCCGT , CM000677.2:g.74719750_74719751insCCGT	GRCh38
NC_000015.9:g.75012091_75012092insCCGT , CM000677.1:g.75012091_75012092insCCGT	GRCh37
NC_000015.8:g.72799144_72799145insCCGT	NCBI36
NG_008431.1:g.2209_2210insCCGT
NG_008431.2:g.2209_2210insCCGT
NG_061374.1:g.10778_10779insACGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379727.8:c.*738_*739insACGG MANE Select	ENSP00000369050.3:n.*738_*739insACGG
ENST00000379727.7:c.*738_*739insACGG	ENSP00000369050.3:n.*738_*739insACGG
ENST00000395048.6:c.*738_*739insACGG	ENSP00000378488.2:n.*738_*739insACGG
ENST00000612821.4:c.2193_2194insACGG	ENSP00000479744.1:n.2193_2194insACGG
ENST00000617691.4:c.*738_*739insACGG	ENSP00000482863.1:n.*738_*739insACGG
NM_000499.3:c.*738_*739insACGG	NP_000490.1:n.*738_*739insACGG
XM_005254185.1:c.*738_*739insACGG	XP_005254242.1:n.*738_*739insACGG
NM_000499.5:c.*738_*739insACGG	NP_000490.1:n.*738_*739insACGG
NM_001319216.2:c.*738_*739insACGG	NP_001306145.1:n.*738_*739insACGG
NM_001319217.2:c.*738_*739insACGG MANE Select	NP_001306146.1:n.*738_*739insACGG