Canonical Allele Identifier: CA2695208538
Gene: TSPAN12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.120788677_120788757del , CM000669.2:g.120788677_120788757del GRCh38
NC_000007.13:g.120428731_120428811del , CM000669.1:g.120428731_120428811del GRCh37
NC_000007.12:g.120215967_120216047del NCBI36
NG_023203.1:g.74367_74447del

Transcript Alleles

HGVS Amino-acid change
ENST00000222747.8:c.753_833del MANE Select ENSP00000222747.3:p.Asp251_Leu278delinsGl...
ENST00000222747.7:c.753_833del ENSP00000222747.3:p.Asp251_Leu278delinsGl...
ENST00000415871.5:c.753_833del ENSP00000397699.1:p.Asp251_Leu278delinsGl...
ENST00000450414.5:c.732_812del ENSP00000397411.1:n.732_812del
NM_012338.3:c.753_833del NP_036470.1:p.Asp251_Leu278delinsGlu
XM_005250239.1:c.753_833del XP_005250296.1:p.Asp251_Leu278delinsGlu
XM_011515993.1:c.753_833del XP_011514295.1:p.Asp251_Leu278delinsGlu
XM_011515994.1:c.753_833del XP_011514296.1:p.Asp251_Leu278delinsGlu
XM_005250239.3:c.753_833del XP_005250296.1:p.Asp251_Leu278delinsGlu
XM_017011913.1:c.678_758del XP_016867402.1:p.Asp226_Leu253delinsGlu
NM_012338.4:c.753_833del MANE Select NP_036470.1:p.Asp251_Leu278delinsGlu