Canonical Allele Identifier: CA2687453876
Gene: CYP7B1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.64604742_64604743insGTAG , CM000670.2:g.64604742_64604743insGTAG GRCh38
NC_000008.10:g.65517299_65517300insGTAG , CM000670.1:g.65517299_65517300insGTAG GRCh37
NC_000008.9:g.65679853_65679854insGTAG NCBI36
NG_008338.1:g.199051_199052insACCT
NG_008338.2:g.199051_199052insACCT

Transcript Alleles

HGVS Amino-acid change
ENST00000310193.4:c.1174_1175insACCT MANE Select ENSP00000310721.3:p.Leu392TyrfsTer13
ENST00000310193.3:c.1174_1175insACCT ENSP00000310721.3:p.Leu392TyrfsTer13
ENST00000523954.1:n.448_449insACCT
NM_004820.3:c.1174_1175insACCT NP_004811.1:p.Leu392TyrfsTer13
NM_001324112.1:c.1174_1175insACCT NP_001311041.1:p.Leu392TyrfsTer13
NM_004820.4:c.1174_1175insACCT NP_004811.1:p.Leu392TyrfsTer13
XM_017014002.1:c.1240_1241insACCT XP_016869491.1:p.Leu414TyrfsTer13
NM_004820.5:c.1174_1175insACCT MANE Select NP_004811.1:p.Leu392TyrfsTer13
NM_001324112.2:c.1174_1175insACCT NP_001311041.1:p.Leu392TyrfsTer13