Canonical Allele Identifier: CA1738876317

Gene: TSPAN12

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788720_120788721delinsTC , CM000669.2:g.120788720_120788721delinsTC	GRCh38
NC_000007.13:g.120428774_120428775delinsTC , CM000669.1:g.120428774_120428775delinsTC	GRCh37
NC_000007.12:g.120216010_120216011delinsTC	NCBI36
NG_023203.1:g.74403_74404delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.789_790delinsGA MANE Select	ENSP00000222747.3:p.Leu263=
ENST00000222747.7:c.789_790delinsGA	ENSP00000222747.3:p.Leu263=
ENST00000415871.5:c.789_790delinsGA	ENSP00000397699.1:p.Leu263=
ENST00000450414.5:c.768_769delinsGA	ENSP00000397411.1:n.768_769delinsGA
NM_012338.3:c.789_790delinsGA	NP_036470.1:p.Leu263=
XM_005250239.1:c.789_790delinsGA	XP_005250296.1:p.Leu263=
XM_011515993.1:c.789_790delinsGA	XP_011514295.1:p.Leu263=
XM_011515994.1:c.789_790delinsGA	XP_011514296.1:p.Leu263=
XM_005250239.3:c.789_790delinsGA	XP_005250296.1:p.Leu263=
XM_017011913.1:c.714_715delinsGA	XP_016867402.1:p.Leu238=
NM_012338.4:c.789_790delinsGA MANE Select	NP_036470.1:p.Leu263=