Canonical Allele Identifier: CA1245628470
Gene: CYP1B1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.38075563_38075568delinsGGAGAA , CM000664.2:g.38075563_38075568delinsGGAGAA GRCh38
NC_000002.11:g.38302706_38302711delinsGGAGAA , CM000664.1:g.38302706_38302711delinsGGAGAA GRCh37
NC_000002.10:g.38156210_38156215delinsGGAGAA NCBI36
NG_008386.2:g.5534_5539delinsTTCTCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000490576.2:c.-1-179_-1-174delinsTTCTCC ENSP00000478839.2:n.-1-179_-1-174delinsTTCTCC
ENST00000610745.5:c.-1-179_-1-174delinsTTCTCC MANE Select ENSP00000478561.1:n.-1-179_-1-174delinsTTCTCC
ENST00000490576.1:c.-1-179_-1-174delinsTTCTCC ENSP00000478839.1:n.-1-179_-1-174delinsTTCTCC
ENST00000494864.1:c.-70-4258_-70-4253delinsTTCTCC ENSP00000479876.1:n.-70-4258_-70-4253delinsTTCTCC
ENST00000610745.4:c.-1-179_-1-174delinsTTCTCC ENSP00000478561.1:n.-1-179_-1-174delinsTTCTCC
ENST00000613082.1:n.375+212_375+217delinsTTCTCC
ENST00000614273.1:c.-1-179_-1-174delinsTTCTCC ENSP00000483678.1:n.-1-179_-1-174delinsTTCTCC
NM_000104.3:c.-1-179_-1-174delinsTTCTCC NP_000095.2:n.-1-179_-1-174delinsTTCTCC
XM_011533236.1:c.177_182delinsGGAGAA XP_011531538.1:p.Leu59=
NM_000104.4:c.-1-179_-1-174delinsTTCTCC MANE Select NP_000095.2:n.-1-179_-1-174delinsTTCTCC