Canonical Allele Identifier: CA2749546754

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075575_38075576insACAC , CM000664.2:g.38075575_38075576insACAC	GRCh38
NC_000002.11:g.38302718_38302719insACAC , CM000664.1:g.38302718_38302719insACAC	GRCh37
NC_000002.10:g.38156222_38156223insACAC	NCBI36
NG_008386.2:g.5526_5527insGTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-187_-1-186insGTGT	ENSP00000478839.2:n.-1-187_-1-186insGTGT
ENST00000610745.5:c.-1-187_-1-186insGTGT MANE Select	ENSP00000478561.1:n.-1-187_-1-186insGTGT
ENST00000490576.1:c.-1-187_-1-186insGTGT	ENSP00000478839.1:n.-1-187_-1-186insGTGT
ENST00000494864.1:c.-70-4266_-70-4265insGTGT	ENSP00000479876.1:n.-70-4266_-70-4265insGTGT
ENST00000610745.4:c.-1-187_-1-186insGTGT	ENSP00000478561.1:n.-1-187_-1-186insGTGT
ENST00000613082.1:n.375+204_375+205insGTGT
ENST00000614273.1:c.-1-187_-1-186insGTGT	ENSP00000483678.1:n.-1-187_-1-186insGTGT
NM_000104.3:c.-1-187_-1-186insGTGT	NP_000095.2:n.-1-187_-1-186insGTGT
XM_011533236.1:c.189_190insACAC	XP_011531538.1:p.Gly64ThrfsTer9
NM_000104.4:c.-1-187_-1-186insGTGT MANE Select	NP_000095.2:n.-1-187_-1-186insGTGT