Canonical Allele Identifier: CA426120753

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 918842
• ClinVar RCV Id: RCV001176675
• dbSNP Id: rs1669284206
• MyVariant Identifiers: chr2:g.48026130T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47798991T>C , CM000664.2:g.47798991T>C	GRCh38
NC_000002.11:g.48026130T>C , CM000664.1:g.48026130T>C	GRCh37
NC_000002.10:g.47879634T>C	NCBI36
NG_007111.1:g.20845T>C , LRG_219:g.20845T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.711T>C (MSH6)	ENSP00000406248.2:p.Thr237=
ENST00000420813.6:c.711T>C (MSH6)	ENSP00000390382.2:p.Thr237=
ENST00000455383.6:c.711T>C (MSH6)	ENSP00000397484.2:p.Thr237=
ENST00000700004.2:c.1008T>C (MSH6)	ENSP00000514752.2:p.Thr336=
ENST00000699999.1:n.1092T>C (MSH6)
ENST00000700000.1:c.1008T>C (MSH6)	ENSP00000514749.1:p.Thr336=
ENST00000700002.1:c.1014T>C (MSH6)	ENSP00000514750.1:p.Thr338=
ENST00000700003.1:c.627+2928T>C (MSH6)	ENSP00000514751.1:n.627+2928T>C
ENST00000700004.1:c.165T>C (MSH6)	ENSP00000514752.1:p.Thr55=
ENST00000234420.11:c.1008T>C (MSH6) MANE Select	ENSP00000234420.5:p.Thr336=
ENST00000540021.6:c.618T>C (MSH6)	ENSP00000446475.1:p.Thr206=
ENST00000652107.1:c.711T>C (MSH6)	ENSP00000498629.1:p.Thr237=
ENST00000673637.1:c.711T>C (MSH6)	ENSP00000501310.1:p.Thr237=
ENST00000234420.9:c.1008T>C (MSH6)	ENSP00000234420.4:p.Thr336=
ENST00000405808.5:c.169+9204A>G (FBXO11)	ENSP00000385127.1:n.169+9204A>G
ENST00000434234.5:c.*124+9003A>G (FBXO11)	ENSP00000402692.1:n.*124+9003A>G
ENST00000445503.5:c.*355T>C (MSH6)	ENSP00000405294.1:n.*355T>C
ENST00000538136.1:c.102T>C (MSH6)	ENSP00000438580.1:p.Thr34=
ENST00000540021.5:c.618T>C (MSH6)	ENSP00000446475.1:p.Thr206=
ENST00000614496.4:c.102T>C (MSH6)	ENSP00000477844.1:p.Thr34=
ENST00000616033.4:c.1005T>C (MSH6)	ENSP00000480261.1:p.Thr335=
ENST00000622629.4:c.-2089T>C (MSH6)	ENSP00000482078.1:n.-2089T>C
NM_000179.2:c.1008T>C , LRG_219t1:c.1008T>C (MSH6)	NP_000170.1:p.Thr336=
NM_001281492.1:c.618T>C (MSH6)	NP_001268421.1:p.Thr206=
NM_001281493.1:c.102T>C (MSH6)	NP_001268422.1:p.Thr34=
NM_001281494.1:c.102T>C (MSH6)	NP_001268423.1:p.Thr34=
XM_005264271.1:c.711T>C (MSH6)	XP_005264328.1:p.Thr237=
XM_011532798.1:c.825T>C (MSH6)	XP_011531100.1:p.Thr275=
XM_011532799.1:c.711T>C (MSH6)	XP_011531101.1:p.Thr237=
XM_011532800.1:c.711T>C (MSH6)	XP_011531102.1:p.Thr237=
XM_024452819.1:c.1008T>C (MSH6)	XP_024308587.1:p.Thr336=
XM_024452820.1:c.825T>C (MSH6)	XP_024308588.1:p.Thr275=
XM_024452821.1:c.711T>C (MSH6)	XP_024308589.1:p.Thr237=
XM_024452822.1:c.102T>C (MSH6)	XP_024308590.1:p.Thr34=
NM_000179.3:c.1008T>C (MSH6) MANE Select	NP_000170.1:p.Thr336=
NM_001281492.2:c.618T>C (MSH6)	NP_001268421.1:p.Thr206=
NM_001281493.2:c.102T>C (MSH6)	NP_001268422.1:p.Thr34=
NM_001281494.2:c.102T>C (MSH6)	NP_001268423.1:p.Thr34=