Canonical Allele Identifier: CA14671540
Gene: USHBP1 HGNC NCBI

Linked Data

dbSNP Id: rs12982178

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.17260759T>C , CM000681.2:g.17260759T>C GRCh38
NC_000019.9:g.17371568T>C , CM000681.1:g.17371568T>C GRCh37
NC_000019.8:g.17232568T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000252597.8:c.643-737A>G MANE Select ENSP00000252597.2:n.643-737A>G
ENST00000252597.7:c.643-737A>G ENSP00000252597.2:n.643-737A>G
ENST00000324554.9:c.643-737A>G ENSP00000324174.5:n.643-737A>G
ENST00000431146.6:c.451-737A>G ENSP00000407902.2:n.451-737A>G
ENST00000597928.5:c.*1447-737A>G ENSP00000469562.1:n.*1447-737A>G
NM_001297703.1:c.451-737A>G NP_001284632.1:n.451-737A>G
NM_031941.3:c.643-737A>G NP_114147.2:n.643-737A>G
XM_005260093.2:c.643-737A>G XP_005260150.1:n.643-737A>G
XM_011528351.1:c.643-737A>G XP_011526653.1:n.643-737A>G
XR_244087.2:n.817-737A>G
NM_001321417.1:c.643-737A>G NP_001308346.1:n.643-737A>G
NR_135632.1:n.817-737A>G
XM_011528351.3:c.643-737A>G XP_011526653.1:n.643-737A>G
NM_001297703.2:c.451-737A>G NP_001284632.1:n.451-737A>G
NM_001321417.2:c.643-737A>G NP_001308346.1:n.643-737A>G
NM_031941.4:c.643-737A>G MANE Select NP_114147.2:n.643-737A>G
NR_135632.2:n.766-737A>G