Canonical Allele Identifier: CA4453781

Gene: TSPAN12

Linked Data

• dbSNP Id: rs144884887
• ExAC: 7:120428670 T / A
• gnomAD v2: 7-120428670-T-A
• MyVariant Identifiers: chr7:g.120428670T>A (hg19) ; chr7:g.120788616T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120788616T>A , CM000669.2:g.120788616T>A	GRCh38
NC_000007.13:g.120428670T>A , CM000669.1:g.120428670T>A	GRCh37
NC_000007.12:g.120215906T>A	NCBI36
NG_023203.1:g.74508A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000222747.8:c.894A>T MANE Select	ENSP00000222747.3:p.Thr298=
ENST00000222747.7:c.894A>T	ENSP00000222747.3:p.Thr298=
ENST00000415871.5:c.894A>T	ENSP00000397699.1:p.Thr298=
ENST00000450414.5:c.873A>T	ENSP00000397411.1:n.873A>T
NM_012338.3:c.894A>T	NP_036470.1:p.Thr298=
XM_005250239.1:c.894A>T	XP_005250296.1:p.Thr298=
XM_011515993.1:c.894A>T	XP_011514295.1:p.Thr298=
XM_011515994.1:c.894A>T	XP_011514296.1:p.Thr298=
XM_005250239.3:c.894A>T	XP_005250296.1:p.Thr298=
XM_017011913.1:c.819A>T	XP_016867402.1:p.Thr273=
NM_012338.4:c.894A>T MANE Select	NP_036470.1:p.Thr298=