Canonical Allele Identifier: CA2777663990
Gene: TSPAN12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120788708del , CM000669.2:g.120788708del GRCh38
NC_000007.13:g.120428762del , CM000669.1:g.120428762del GRCh37
NC_000007.12:g.120215998del NCBI36
NG_023203.1:g.74416del

Transcript Alleles

HGVS Amino-acid Change
ENST00000222747.8:c.802del MANE Select ENSP00000222747.3:p.Ser268LeufsTer9
ENST00000222747.7:c.802del ENSP00000222747.3:p.Ser268LeufsTer9
ENST00000415871.5:c.802del ENSP00000397699.1:p.Ser268LeufsTer9
ENST00000450414.5:c.781del ENSP00000397411.1:n.781del
NM_012338.3:c.802del NP_036470.1:p.Ser268LeufsTer9
XM_005250239.1:c.802del XP_005250296.1:p.Ser268LeufsTer9
XM_011515993.1:c.802del XP_011514295.1:p.Ser268LeufsTer9
XM_011515994.1:c.802del XP_011514296.1:p.Ser268LeufsTer9
XM_005250239.3:c.802del XP_005250296.1:p.Ser268LeufsTer9
XM_017011913.1:c.727del XP_016867402.1:p.Ser243LeufsTer9
NM_012338.4:c.802del MANE Select NP_036470.1:p.Ser268LeufsTer9
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