Canonical Allele Identifier: CA14159158
Gene: SPTBN5 HGNC NCBI

Linked Data

dbSNP Id: rs4923918

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41868745G>A , CM000677.2:g.41868745G>A GRCh38
NC_000015.9:g.42160943G>A , CM000677.1:g.42160943G>A GRCh37
NC_000015.8:g.39948235G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000320955.8:c.5854-144C>T MANE Select ENSP00000317790.6:n.5854-144C>T
ENST00000320955.7:c.5854-144C>T ENSP00000317790.6:n.5854-144C>T
NM_016642.3:c.5854-144C>T NP_057726.4:n.5854-144C>T
XM_017022299.1:c.5914-144C>T XP_016877788.1:n.5914-144C>T
XM_017022300.1:c.5914-144C>T XP_016877789.1:n.5914-144C>T
XM_017022301.1:c.5038-144C>T XP_016877790.1:n.5038-144C>T
XM_017022302.1:c.3091-144C>T XP_016877791.1:n.3091-144C>T
XM_017022303.1:c.5914-144C>T XP_016877792.1:n.5914-144C>T
XM_017022304.1:c.5914-144C>T XP_016877793.1:n.5914-144C>T
XR_001751302.1:n.5940-144C>T
XR_001751303.1:n.5940-144C>T
XR_001751304.1:n.5940-144C>T
XR_001751305.1:n.5940-144C>T
NM_016642.4:c.5854-144C>T MANE Select NP_057726.4:n.5854-144C>T