Canonical Allele Identifier: CA2749546730

Gene: CYP1B1

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.38075542_38075543insCTT , CM000664.2:g.38075542_38075543insCTT	GRCh38
NC_000002.11:g.38302685_38302686insCTT , CM000664.1:g.38302685_38302686insCTT	GRCh37
NC_000002.10:g.38156189_38156190insCTT	NCBI36
NG_008386.2:g.5559_5560insAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000490576.2:c.-1-154_-1-153insAAG	ENSP00000478839.2:n.-1-154_-1-153insAAG
ENST00000610745.5:c.-1-154_-1-153insAAG MANE Select	ENSP00000478561.1:n.-1-154_-1-153insAAG
ENST00000490576.1:c.-1-154_-1-153insAAG	ENSP00000478839.1:n.-1-154_-1-153insAAG
ENST00000494864.1:c.-70-4233_-70-4232insAAG	ENSP00000479876.1:n.-70-4233_-70-4232insAAG
ENST00000610745.4:c.-1-154_-1-153insAAG	ENSP00000478561.1:n.-1-154_-1-153insAAG
ENST00000613082.1:n.375+237_375+238insAAG
ENST00000614273.1:c.-1-154_-1-153insAAG	ENSP00000483678.1:n.-1-154_-1-153insAAG
NM_000104.3:c.-1-154_-1-153insAAG	NP_000095.2:n.-1-154_-1-153insAAG
XM_011533236.1:c.156_157insCTT	XP_011531538.1:p.Pro52_Ser53insLeu
NM_000104.4:c.-1-154_-1-153insAAG MANE Select	NP_000095.2:n.-1-154_-1-153insAAG