Canonical Allele Identifier: CA2684641443

Gene: TSPAN12

Linked Data

• gnomAD v4: 7-120788609-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788612dup , CM000669.2:g.120788612dup	GRCh38
NC_000007.13:g.120428666dup , CM000669.1:g.120428666dup	GRCh37
NC_000007.12:g.120215902dup	NCBI36
NG_023203.1:g.74514dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.900dup MANE Select	ENSP00000222747.3:p.Glu301Ter
ENST00000222747.7:c.900dup	ENSP00000222747.3:p.Glu301Ter
ENST00000415871.5:c.900dup	ENSP00000397699.1:p.Glu301Ter
ENST00000450414.5:c.879dup	ENSP00000397411.1:n.879dup
NM_012338.3:c.900dup	NP_036470.1:p.Glu301Ter
XM_005250239.1:c.900dup	XP_005250296.1:p.Glu301Ter
XM_011515993.1:c.900dup	XP_011514295.1:p.Glu301Ter
XM_011515994.1:c.900dup	XP_011514296.1:p.Glu301Ter
XM_005250239.3:c.900dup	XP_005250296.1:p.Glu301Ter
XM_017011913.1:c.825dup	XP_016867402.1:p.Glu276Ter
NM_012338.4:c.900dup MANE Select	NP_036470.1:p.Glu301Ter