Canonical Allele Identifier: CA369141488

Gene: TSPAN12

Linked Data

• dbSNP Id: rs1218342723
• gnomAD v2: 7-120480091-C-A
• MyVariant Identifiers: chr7:g.120480091C>A (hg19) ; chr7:g.120840037C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120840037C>A , CM000669.2:g.120840037C>A	GRCh38
NC_000007.13:g.120480091C>A , CM000669.1:g.120480091C>A	GRCh37
NC_000007.12:g.120267327C>A	NCBI36
NG_023203.1:g.23087G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.139G>T MANE Select	ENSP00000222747.3:p.Ala47Ser
ENST00000222747.7:c.139G>T	ENSP00000222747.3:p.Ala47Ser
ENST00000415871.5:c.139G>T	ENSP00000397699.1:p.Ala47Ser
ENST00000424710.5:c.139G>T	ENSP00000404942.1:p.Ala47Ser
ENST00000430985.1:c.139G>T	ENSP00000388819.1:p.Ala47Ser
ENST00000433758.5:c.139G>T	ENSP00000399059.1:p.Ala47Ser
ENST00000441017.5:c.139G>T	ENSP00000411158.1:p.Ala47Ser
NM_012338.3:c.139G>T	NP_036470.1:p.Ala47Ser
XM_005250239.1:c.139G>T	XP_005250296.1:p.Ala47Ser
XM_011515993.1:c.139G>T	XP_011514295.1:p.Ala47Ser
XM_011515994.1:c.139G>T	XP_011514296.1:p.Ala47Ser
XM_005250239.3:c.139G>T	XP_005250296.1:p.Ala47Ser
XM_017011913.1:c.139G>T	XP_016867402.1:p.Ala47Ser
NM_012338.4:c.139G>T MANE Select	NP_036470.1:p.Ala47Ser