Canonical Allele Identifier: CA1738876275

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788704_120788706delinsTGA , CM000669.2:g.120788704_120788706delinsTGA	GRCh38
NC_000007.13:g.120428758_120428760delinsTGA , CM000669.1:g.120428758_120428760delinsTGA	GRCh37
NC_000007.12:g.120215994_120215996delinsTGA	NCBI36
NG_023203.1:g.74418_74420delinsTCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.804_806delinsTCA MANE Select	ENSP00000222747.3:p.Ser268=
ENST00000222747.7:c.804_806delinsTCA	ENSP00000222747.3:p.Ser268=
ENST00000415871.5:c.804_806delinsTCA	ENSP00000397699.1:p.Ser268=
ENST00000450414.5:c.783_785delinsTCA	ENSP00000397411.1:n.783_785delinsTCA
NM_012338.3:c.804_806delinsTCA	NP_036470.1:p.Ser268=
XM_005250239.1:c.804_806delinsTCA	XP_005250296.1:p.Ser268=
XM_011515993.1:c.804_806delinsTCA	XP_011514295.1:p.Ser268=
XM_011515994.1:c.804_806delinsTCA	XP_011514296.1:p.Ser268=
XM_005250239.3:c.804_806delinsTCA	XP_005250296.1:p.Ser268=
XM_017011913.1:c.729_731delinsTCA	XP_016867402.1:p.Ser243=
NM_012338.4:c.804_806delinsTCA MANE Select	NP_036470.1:p.Ser268=