Canonical Allele Identifier: CA457397868

Gene: TSPAN12

Linked Data

• MyVariant Identifiers: chr7:g.120480095T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.120840041T>C , CM000669.2:g.120840041T>C	GRCh38
NC_000007.13:g.120480095T>C , CM000669.1:g.120480095T>C	GRCh37
NC_000007.12:g.120267331T>C	NCBI36
NG_023203.1:g.23083A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000222747.8:c.135A>G MANE Select	ENSP00000222747.3:p.Leu45=
ENST00000222747.7:c.135A>G	ENSP00000222747.3:p.Leu45=
ENST00000415871.5:c.135A>G	ENSP00000397699.1:p.Leu45=
ENST00000424710.5:c.135A>G	ENSP00000404942.1:p.Leu45=
ENST00000430985.1:c.135A>G	ENSP00000388819.1:p.Leu45=
ENST00000433758.5:c.135A>G	ENSP00000399059.1:p.Leu45=
ENST00000441017.5:c.135A>G	ENSP00000411158.1:p.Leu45=
NM_012338.3:c.135A>G	NP_036470.1:p.Leu45=
XM_005250239.1:c.135A>G	XP_005250296.1:p.Leu45=
XM_011515993.1:c.135A>G	XP_011514295.1:p.Leu45=
XM_011515994.1:c.135A>G	XP_011514296.1:p.Leu45=
XM_005250239.3:c.135A>G	XP_005250296.1:p.Leu45=
XM_017011913.1:c.135A>G	XP_016867402.1:p.Leu45=
NM_012338.4:c.135A>G MANE Select	NP_036470.1:p.Leu45=