Canonical Allele Identifier: CA2266216446
Gene: STXBP4 HGNC NCBI

Linked Data

dbSNP Id: rs2787486

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.55132413A>T , CM000679.2:g.55132413A>T GRCh38
NC_000017.10:g.53209774A>T , CM000679.1:g.53209774A>T GRCh37
NC_000017.9:g.50564773A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376352.6:c.1490-8897A>T MANE Select ENSP00000365530.2:n.1490-8897A>T
ENST00000434978.6:c.1424-8897A>T ENSP00000391087.2:n.1424-8897A>T
NM_178509.5:c.1490-8897A>T NP_848604.3:n.1490-8897A>T
XM_005257187.3:c.1496-8897A>T XP_005257244.1:n.1496-8897A>T
XM_011524581.1:c.1505-8897A>T XP_011522883.1:n.1505-8897A>T
XM_011524582.1:c.1499-8897A>T XP_011522884.1:n.1499-8897A>T
XM_011524583.1:c.1424-8897A>T XP_011522885.1:n.1424-8897A>T
XM_005257187.4:c.1496-8897A>T XP_005257244.1:n.1496-8897A>T
XM_017024410.1:c.1544-8897A>T XP_016879899.1:n.1544-8897A>T
XM_017024411.2:c.1538-8897A>T XP_016879900.1:n.1538-8897A>T
XM_017024413.1:c.1313-8897A>T XP_016879902.1:n.1313-8897A>T
NM_178509.6:c.1490-8897A>T MANE Select NP_848604.3:n.1490-8897A>T
NM_001398481.1:c.1496-8897A>T NP_001385410.1:n.1496-8897A>T