Canonical Allele Identifier: CA10578139

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 233674
• ClinVar RCV Id: RCV000214591 ; RCV001854702 ; RCV002472974 ; RCV003998571
• dbSNP Id: rs876660564
• MyVariant Identifiers: chr2:g.48030679G>A (hg19) ; chr2:g.47803540G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47803540G>A , CM000664.2:g.47803540G>A	GRCh38
NC_000002.11:g.48030679G>A , CM000664.1:g.48030679G>A	GRCh37
NC_000002.10:g.47884183G>A	NCBI36
NG_007111.1:g.25394G>A , LRG_219:g.25394G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.2996G>A (MSH6)	ENSP00000406248.2:p.Cys999Tyr
ENST00000420813.6:c.2996G>A (MSH6)	ENSP00000390382.2:p.Cys999Tyr
ENST00000455383.6:c.2996G>A (MSH6)	ENSP00000397484.2:p.Cys999Tyr
ENST00000700004.2:c.3173-2078G>A (MSH6)	ENSP00000514752.2:n.3173-2078G>A
ENST00000699999.1:n.3377G>A (MSH6)
ENST00000700000.1:c.1727G>A (MSH6)	ENSP00000514749.1:p.Cys576Tyr
ENST00000700002.1:c.3299G>A (MSH6)	ENSP00000514750.1:p.Cys1100Tyr
ENST00000700003.1:c.748G>A (MSH6)	ENSP00000514751.1:n.748G>A
ENST00000700004.1:c.2330-2078G>A (MSH6)	ENSP00000514752.1:n.2330-2078G>A
ENST00000700005.1:n.2144G>A (MSH6)
ENST00000700006.1:n.2141G>A (MSH6)
ENST00000700007.1:n.1298G>A (MSH6)
ENST00000700008.1:n.872G>A (MSH6)
ENST00000700009.1:n.871G>A (MSH6)
ENST00000700010.1:n.702G>A (MSH6)
ENST00000700011.1:n.773G>A (MSH6)
ENST00000234420.11:c.3293G>A (MSH6) MANE Select	ENSP00000234420.5:p.Cys1098Tyr
ENST00000540021.6:c.2903G>A (MSH6)	ENSP00000446475.1:p.Cys968Tyr
ENST00000652107.1:c.2996G>A (MSH6)	ENSP00000498629.1:p.Cys999Tyr
ENST00000673637.1:c.2996G>A (MSH6)	ENSP00000501310.1:p.Cys999Tyr
ENST00000234420.9:c.3293G>A (MSH6)	ENSP00000234420.4:p.Cys1098Tyr
ENST00000405808.5:c.169+4655C>T (FBXO11)	ENSP00000385127.1:n.169+4655C>T
ENST00000434234.5:c.*124+4454C>T (FBXO11)	ENSP00000402692.1:n.*124+4454C>T
ENST00000445503.5:c.*2640G>A (MSH6)	ENSP00000405294.1:n.*2640G>A
ENST00000538136.1:c.2387G>A (MSH6)	ENSP00000438580.1:p.Cys796Tyr
ENST00000540021.5:c.2903G>A (MSH6)	ENSP00000446475.1:p.Cys968Tyr
ENST00000614496.4:c.2387G>A (MSH6)	ENSP00000477844.1:p.Cys796Tyr
ENST00000622629.4:c.197G>A (MSH6)	ENSP00000482078.1:p.Cys66Tyr
NM_000179.2:c.3293G>A , LRG_219t1:c.3293G>A (MSH6)	NP_000170.1:p.Cys1098Tyr
NM_001281492.1:c.2903G>A (MSH6)	NP_001268421.1:p.Cys968Tyr
NM_001281493.1:c.2387G>A (MSH6)	NP_001268422.1:p.Cys796Tyr
NM_001281494.1:c.2387G>A (MSH6)	NP_001268423.1:p.Cys796Tyr
XM_005264271.1:c.2996G>A (MSH6)	XP_005264328.1:p.Cys999Tyr
XM_011532798.1:c.3110G>A (MSH6)	XP_011531100.1:p.Cys1037Tyr
XM_011532799.1:c.2996G>A (MSH6)	XP_011531101.1:p.Cys999Tyr
XM_011532800.1:c.2996G>A (MSH6)	XP_011531102.1:p.Cys999Tyr
XM_024452819.1:c.3293G>A (MSH6)	XP_024308587.1:p.Cys1098Tyr
XM_024452820.1:c.3110G>A (MSH6)	XP_024308588.1:p.Cys1037Tyr
XM_024452821.1:c.2996G>A (MSH6)	XP_024308589.1:p.Cys999Tyr
XM_024452822.1:c.2387G>A (MSH6)	XP_024308590.1:p.Cys796Tyr
NM_000179.3:c.3293G>A (MSH6) MANE Select	NP_000170.1:p.Cys1098Tyr
NM_001281492.2:c.2903G>A (MSH6)	NP_001268421.1:p.Cys968Tyr
NM_001281493.2:c.2387G>A (MSH6)	NP_001268422.1:p.Cys796Tyr
NM_001281494.2:c.2387G>A (MSH6)	NP_001268423.1:p.Cys796Tyr