Canonical Allele Identifier: CA376215932
Gene: STAM HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17714562C>G , CM000672.2:g.17714562C>G GRCh38
NC_000010.10:g.17756561C>G , CM000672.1:g.17756561C>G GRCh37
NC_000010.9:g.17796567C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377524.8:c.1405C>G MANE Select ENSP00000366746.3:p.Gln469Glu
ENST00000377524.7:c.1405C>G ENSP00000366746.3:p.Gln469Glu
NM_003473.3:c.1405C>G NP_003464.1:p.Gln469Glu
NR_037774.1:n.1448C>G
XM_005252603.2:c.1255C>G XP_005252660.1:p.Gln419Glu
NM_001324282.1:c.1309C>G NP_001311211.1:p.Gln437Glu
NM_001324283.1:c.1255C>G NP_001311212.1:p.Gln419Glu
NM_001324284.1:c.1255C>G NP_001311213.1:p.Gln419Glu
NM_001324285.1:c.1255C>G NP_001311214.1:p.Gln419Glu
NM_001324286.1:c.1114C>G NP_001311215.1:p.Gln372Glu
NM_001324287.1:c.1072C>G NP_001311216.1:p.Gln358Glu
NM_001324288.1:c.1021C>G NP_001311217.1:p.Gln341Glu
NM_001324289.1:c.1021C>G NP_001311218.1:p.Gln341Glu
XM_017016685.2:c.1021C>G XP_016872174.1:p.Gln341Glu
NM_003473.4:c.1405C>G MANE Select NP_003464.1:p.Gln469Glu
NM_001324282.2:c.1309C>G NP_001311211.1:p.Gln437Glu
NM_001324283.2:c.1255C>G NP_001311212.1:p.Gln419Glu
NM_001324284.2:c.1255C>G NP_001311213.1:p.Gln419Glu
NM_001324285.2:c.1255C>G NP_001311214.1:p.Gln419Glu
NM_001324286.2:c.1114C>G NP_001311215.1:p.Gln372Glu
NM_001324287.2:c.1072C>G NP_001311216.1:p.Gln358Glu
NM_001324288.2:c.1021C>G NP_001311217.1:p.Gln341Glu
NM_001324289.2:c.1021C>G NP_001311218.1:p.Gln341Glu