Canonical Allele Identifier: CA369133494

Gene: TSPAN12

Linked Data

• MyVariant Identifiers: chr7:g.120428762A>T (hg19) ; chr7:g.120788708A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788708A>T , CM000669.2:g.120788708A>T	GRCh38
NC_000007.13:g.120428762A>T , CM000669.1:g.120428762A>T	GRCh37
NC_000007.12:g.120215998A>T	NCBI36
NG_023203.1:g.74416T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.802T>A MANE Select	ENSP00000222747.3:p.Ser268Thr
ENST00000222747.7:c.802T>A	ENSP00000222747.3:p.Ser268Thr
ENST00000415871.5:c.802T>A	ENSP00000397699.1:p.Ser268Thr
ENST00000450414.5:c.781T>A	ENSP00000397411.1:n.781T>A
NM_012338.3:c.802T>A	NP_036470.1:p.Ser268Thr
XM_005250239.1:c.802T>A	XP_005250296.1:p.Ser268Thr
XM_011515993.1:c.802T>A	XP_011514295.1:p.Ser268Thr
XM_011515994.1:c.802T>A	XP_011514296.1:p.Ser268Thr
XM_005250239.3:c.802T>A	XP_005250296.1:p.Ser268Thr
XM_017011913.1:c.727T>A	XP_016867402.1:p.Ser243Thr
NM_012338.4:c.802T>A MANE Select	NP_036470.1:p.Ser268Thr