Canonical Allele Identifier: CA369137467

Gene: TSPAN12

Linked Data

• MyVariant Identifiers: chr7:g.120450569C>T (hg19) ; chr7:g.120810515C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120810515C>T , CM000669.2:g.120810515C>T	GRCh38
NC_000007.13:g.120450569C>T , CM000669.1:g.120450569C>T	GRCh37
NC_000007.12:g.120237805C>T	NCBI36
NG_023203.1:g.52609G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.416G>A MANE Select	ENSP00000222747.3:p.Gly139Glu
ENST00000222747.7:c.416G>A	ENSP00000222747.3:p.Gly139Glu
ENST00000415871.5:c.416G>A	ENSP00000397699.1:p.Gly139Glu
ENST00000441017.5:c.416G>A	ENSP00000411158.1:p.Gly139Glu
ENST00000450414.5:c.395G>A	ENSP00000397411.1:n.395G>A
NM_012338.3:c.416G>A	NP_036470.1:p.Gly139Glu
XM_005250239.1:c.416G>A	XP_005250296.1:p.Gly139Glu
XM_011515993.1:c.416G>A	XP_011514295.1:p.Gly139Glu
XM_011515994.1:c.416G>A	XP_011514296.1:p.Gly139Glu
XM_005250239.3:c.416G>A	XP_005250296.1:p.Gly139Glu
XM_017011913.1:c.341G>A	XP_016867402.1:p.Gly114Glu
NM_012338.4:c.416G>A MANE Select	NP_036470.1:p.Gly139Glu