Canonical Allele Identifier: CA1738882788

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120839969_120839970delinsAG , CM000669.2:g.120839969_120839970delinsAG	GRCh38
NC_000007.13:g.120480023_120480024delinsAG , CM000669.1:g.120480023_120480024delinsAG	GRCh37
NC_000007.12:g.120267259_120267260delinsAG	NCBI36
NG_023203.1:g.23154_23155delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.149+57_149+58delinsCT MANE Select	ENSP00000222747.3:n.149+57_149+58delinsCT
ENST00000222747.7:c.149+57_149+58delinsCT	ENSP00000222747.3:n.149+57_149+58delinsCT
ENST00000415871.5:c.149+57_149+58delinsCT	ENSP00000397699.1:n.149+57_149+58delinsCT
ENST00000424710.5:c.149+57_149+58delinsCT	ENSP00000404942.1:n.149+57_149+58delinsCT
ENST00000430985.1:c.149+57_149+58delinsCT	ENSP00000388819.1:n.149+57_149+58delinsCT
ENST00000433758.5:c.149+57_149+58delinsCT	ENSP00000399059.1:n.149+57_149+58delinsCT
ENST00000441017.5:c.149+57_149+58delinsCT	ENSP00000411158.1:n.149+57_149+58delinsCT
NM_012338.3:c.149+57_149+58delinsCT	NP_036470.1:n.149+57_149+58delinsCT
XM_005250239.1:c.149+57_149+58delinsCT	XP_005250296.1:n.149+57_149+58delinsCT
XM_011515993.1:c.149+57_149+58delinsCT	XP_011514295.1:n.149+57_149+58delinsCT
XM_011515994.1:c.149+57_149+58delinsCT	XP_011514296.1:n.149+57_149+58delinsCT
XM_005250239.3:c.149+57_149+58delinsCT	XP_005250296.1:n.149+57_149+58delinsCT
XM_017011913.1:c.149+57_149+58delinsCT	XP_016867402.1:n.149+57_149+58delinsCT
NM_012338.4:c.149+57_149+58delinsCT MANE Select	NP_036470.1:n.149+57_149+58delinsCT