Canonical Allele Identifier: CA396602673

Gene: MTSS2

Linked Data

• ClinVar Variation Id: 2490484
• ClinVar RCV Id: RCV004276041
• MyVariant Identifiers: chr16:g.70708337T>C (hg19) ; chr16:g.70674434T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.70674434T>C , CM000678.2:g.70674434T>C	GRCh38
NC_000016.9:g.70708337T>C , CM000678.1:g.70708337T>C	GRCh37
NC_000016.8:g.69265838T>C	NCBI36
NG_051360.1:g.16618A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000338779.11:c.925A>G MANE Select	ENSP00000341171.6:p.Ser309Gly
ENST00000338779.10:c.925A>G	ENSP00000341171.6:p.Ser309Gly
ENST00000562883.6:c.295-2A>G
ENST00000616026.4:c.922A>G	ENSP00000481169.1:p.Ser308Gly
NM_138383.2:c.925A>G	NP_612392.1:p.Ser309Gly
XM_005256236.3:c.822-2A>G	XP_005256293.1:n.822-2A>G
XM_011523450.1:c.1000A>G	XP_011521752.1:p.Ser334Gly
XM_011523451.1:c.991A>G	XP_011521753.1:p.Ser331Gly
XM_011523452.1:c.1000A>G	XP_011521754.1:p.Ser334Gly
XM_011523453.1:c.925A>G	XP_011521755.1:p.Ser309Gly
XM_011523454.1:c.916A>G	XP_011521756.1:p.Ser306Gly
XM_011523455.1:c.906-2A>G	XP_011521757.1:n.906-2A>G
XM_011523456.1:c.1000A>G	XP_011521758.1:p.Ser334Gly
XM_011523457.1:c.1035+2447A>G	XP_011521759.1:n.1035+2447A>G
XM_011523458.1:c.481A>G	XP_011521760.1:p.Ser161Gly
XM_011523459.1:c.1000A>G	XP_011521761.1:p.Ser334Gly
XR_933483.1:n.1016+2447A>G
XM_005256236.5:c.822-2A>G	XP_005256293.3:n.822-2A>G
XM_011523450.2:c.1000A>G	XP_011521752.1:p.Ser334Gly
XM_011523453.3:c.925A>G	XP_011521755.3:p.Ser309Gly
XM_011523454.3:c.916A>G	XP_011521756.3:p.Ser306Gly
XM_011523458.2:c.481A>G	XP_011521760.1:p.Ser161Gly
XM_017023879.2:c.831-2A>G	XP_016879368.2:n.831-2A>G
XM_017023880.2:c.925A>G	XP_016879369.2:p.Ser309Gly
XM_017023881.2:c.831-2A>G	XP_016879370.2:n.831-2A>G
XM_017023882.2:c.925A>G	XP_016879371.2:p.Ser309Gly
XM_017023883.2:c.925A>G	XP_016879372.2:p.Ser309Gly
NM_138383.3:c.925A>G MANE Select	NP_612392.1:p.Ser309Gly