Canonical Allele Identifier: CA346738651

Gene: MSH6 FBXO11

Linked Data

• gnomAD v4: 2-47795938-G-T
• MyVariant Identifiers: chr2:g.48023077G>T (hg19) ; chr2:g.47795938G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47795938G>T , CM000664.2:g.47795938G>T	GRCh38
NC_000002.11:g.48023077G>T , CM000664.1:g.48023077G>T	GRCh37
NC_000002.10:g.47876581G>T	NCBI36
NG_007111.1:g.17792G>T , LRG_219:g.17792G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000411819.2:c.205G>T (MSH6)	ENSP00000406248.2:p.Ala69Ser
ENST00000420813.6:c.205G>T (MSH6)	ENSP00000390382.2:p.Ala69Ser
ENST00000455383.6:c.205G>T (MSH6)	ENSP00000397484.2:p.Ala69Ser
ENST00000700004.2:c.502G>T (MSH6)	ENSP00000514752.2:p.Ala168Ser
ENST00000699999.1:n.586G>T (MSH6)
ENST00000700000.1:c.502G>T (MSH6)	ENSP00000514749.1:p.Ala168Ser
ENST00000700001.1:n.574G>T (MSH6)
ENST00000700002.1:c.502G>T (MSH6)	ENSP00000514750.1:p.Ala168Ser
ENST00000700003.1:c.502G>T (MSH6)	ENSP00000514751.1:p.Ala168Ser
ENST00000234420.11:c.502G>T (MSH6) MANE Select	ENSP00000234420.5:p.Ala168Ser
ENST00000540021.6:c.238-2673G>T (MSH6)	ENSP00000446475.1:n.238-2673G>T
ENST00000652107.1:c.205G>T (MSH6)	ENSP00000498629.1:p.Ala69Ser
ENST00000673637.1:c.205G>T (MSH6)	ENSP00000501310.1:p.Ala69Ser
ENST00000673922.1:n.350-2673G>T (MSH6)
ENST00000234420.9:c.502G>T (MSH6)	ENSP00000234420.4:p.Ala168Ser
ENST00000405808.5:c.170-6498C>A (FBXO11)	ENSP00000385127.1:n.170-6498C>A
ENST00000411819.1:c.205G>T (MSH6)	ENSP00000406248.1:p.Ala69Ser
ENST00000420813.5:c.205G>T (MSH6)	ENSP00000390382.1:p.Ala69Ser
ENST00000434234.5:c.*125-6498C>A (FBXO11)	ENSP00000402692.1:n.*125-6498C>A
ENST00000445503.5:c.458-2673G>T (MSH6)	ENSP00000405294.1:n.458-2673G>T
ENST00000455383.5:c.205G>T (MSH6)	ENSP00000397484.1:p.Ala69Ser
ENST00000456246.1:c.305G>T (MSH6)	ENSP00000410570.1:p.Cys102Phe
ENST00000538136.1:c.-401G>T (MSH6)	ENSP00000438580.1:n.-401G>T
ENST00000540021.5:c.238-2673G>T (MSH6)	ENSP00000446475.1:n.238-2673G>T
ENST00000614496.4:c.-279-2673G>T (MSH6)	ENSP00000477844.1:n.-279-2673G>T
ENST00000616033.4:c.499G>T (MSH6)	ENSP00000480261.1:p.Ala167Ser
ENST00000622629.4:c.-2595G>T (MSH6)	ENSP00000482078.1:n.-2595G>T
NM_000179.2:c.502G>T , LRG_219t1:c.502G>T (MSH6)	NP_000170.1:p.Ala168Ser
NM_001281492.1:c.238-2673G>T (MSH6)	NP_001268421.1:n.238-2673G>T
NM_001281493.1:c.-279-2673G>T (MSH6)	NP_001268422.1:n.-279-2673G>T
NM_001281494.1:c.-401G>T (MSH6)	NP_001268423.1:n.-401G>T
XM_005264271.1:c.205G>T (MSH6)	XP_005264328.1:p.Ala69Ser
XM_011532798.1:c.319G>T (MSH6)	XP_011531100.1:p.Ala107Ser
XM_011532799.1:c.205G>T (MSH6)	XP_011531101.1:p.Ala69Ser
XM_011532800.1:c.205G>T (MSH6)	XP_011531102.1:p.Ala69Ser
XM_024452819.1:c.502G>T (MSH6)	XP_024308587.1:p.Ala168Ser
XM_024452820.1:c.319G>T (MSH6)	XP_024308588.1:p.Ala107Ser
XM_024452821.1:c.205G>T (MSH6)	XP_024308589.1:p.Ala69Ser
XM_024452822.1:c.-279-2673G>T (MSH6)	XP_024308590.1:n.-279-2673G>T
NM_000179.3:c.502G>T (MSH6) MANE Select	NP_000170.1:p.Ala168Ser
NM_001281492.2:c.238-2673G>T (MSH6)	NP_001268421.1:n.238-2673G>T
NM_001281493.2:c.-279-2673G>T (MSH6)	NP_001268422.1:n.-279-2673G>T
NM_001281494.2:c.-401G>T (MSH6)	NP_001268423.1:n.-401G>T