Canonical Allele Identifier: CA2749546748

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075563_38075564insAGT , CM000664.2:g.38075563_38075564insAGT	GRCh38
NC_000002.11:g.38302706_38302707insAGT , CM000664.1:g.38302706_38302707insAGT	GRCh37
NC_000002.10:g.38156210_38156211insAGT	NCBI36
NG_008386.2:g.5538_5539insACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-175_-1-174insACT	ENSP00000478839.2:n.-1-175_-1-174insACT
ENST00000610745.5:c.-1-175_-1-174insACT MANE Select	ENSP00000478561.1:n.-1-175_-1-174insACT
ENST00000490576.1:c.-1-175_-1-174insACT	ENSP00000478839.1:n.-1-175_-1-174insACT
ENST00000494864.1:c.-70-4254_-70-4253insACT	ENSP00000479876.1:n.-70-4254_-70-4253insACT
ENST00000610745.4:c.-1-175_-1-174insACT	ENSP00000478561.1:n.-1-175_-1-174insACT
ENST00000613082.1:n.375+216_375+217insACT
ENST00000614273.1:c.-1-175_-1-174insACT	ENSP00000483678.1:n.-1-175_-1-174insACT
NM_000104.3:c.-1-175_-1-174insACT	NP_000095.2:n.-1-175_-1-174insACT
XM_011533236.1:c.177_178insAGT	XP_011531538.1:p.Leu59_Glu60insSer
NM_000104.4:c.-1-175_-1-174insACT MANE Select	NP_000095.2:n.-1-175_-1-174insACT