Canonical Allele Identifier: CA16604182

Gene: MSH6 FBXO11

Linked Data

• ClinVar Variation Id: 381229
• ClinVar RCV Id: RCV000426053 ; RCV001435788 ; RCV002411321
• dbSNP Id: rs1057520981
• gnomAD v4: 2-47799789-A-C
• MyVariant Identifiers: chr2:g.48026928A>C (hg19) ; chr2:g.47799789A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799789A>C , CM000664.2:g.47799789A>C	GRCh38
NC_000002.11:g.48026928A>C , CM000664.1:g.48026928A>C	GRCh37
NC_000002.10:g.47880432A>C	NCBI36
NG_007111.1:g.21643A>C , LRG_219:g.21643A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.1509A>C (MSH6)	ENSP00000406248.2:p.Ser503=
ENST00000420813.6:c.1509A>C (MSH6)	ENSP00000390382.2:p.Ser503=
ENST00000455383.6:c.1509A>C (MSH6)	ENSP00000397484.2:p.Ser503=
ENST00000700004.2:c.1806A>C (MSH6)	ENSP00000514752.2:p.Ser602=
ENST00000699999.1:n.1890A>C (MSH6)
ENST00000700000.1:c.1606+200A>C (MSH6)	ENSP00000514749.1:n.1606+200A>C
ENST00000700002.1:c.1812A>C (MSH6)	ENSP00000514750.1:p.Ser604=
ENST00000700003.1:c.628-3631A>C (MSH6)	ENSP00000514751.1:n.628-3631A>C
ENST00000700004.1:c.963A>C (MSH6)	ENSP00000514752.1:p.Ser321=
ENST00000234420.11:c.1806A>C (MSH6) MANE Select	ENSP00000234420.5:p.Ser602=
ENST00000540021.6:c.1416A>C (MSH6)	ENSP00000446475.1:p.Ser472=
ENST00000652107.1:c.1509A>C (MSH6)	ENSP00000498629.1:p.Ser503=
ENST00000673637.1:c.1509A>C (MSH6)	ENSP00000501310.1:p.Ser503=
ENST00000234420.9:c.1806A>C (MSH6)	ENSP00000234420.4:p.Ser602=
ENST00000405808.5:c.169+8406T>G (FBXO11)	ENSP00000385127.1:n.169+8406T>G
ENST00000434234.5:c.*124+8205T>G (FBXO11)	ENSP00000402692.1:n.*124+8205T>G
ENST00000445503.5:c.*1153A>C (MSH6)	ENSP00000405294.1:n.*1153A>C
ENST00000538136.1:c.900A>C (MSH6)	ENSP00000438580.1:p.Ser300=
ENST00000540021.5:c.1416A>C (MSH6)	ENSP00000446475.1:p.Ser472=
ENST00000614496.4:c.900A>C (MSH6)	ENSP00000477844.1:p.Ser300=
ENST00000616033.4:c.1803A>C (MSH6)	ENSP00000480261.1:p.Ser601=
ENST00000622629.4:c.-1291A>C (MSH6)	ENSP00000482078.1:n.-1291A>C
NM_000179.2:c.1806A>C , LRG_219t1:c.1806A>C (MSH6)	NP_000170.1:p.Ser602=
NM_001281492.1:c.1416A>C (MSH6)	NP_001268421.1:p.Ser472=
NM_001281493.1:c.900A>C (MSH6)	NP_001268422.1:p.Ser300=
NM_001281494.1:c.900A>C (MSH6)	NP_001268423.1:p.Ser300=
XM_005264271.1:c.1509A>C (MSH6)	XP_005264328.1:p.Ser503=
XM_011532798.1:c.1623A>C (MSH6)	XP_011531100.1:p.Ser541=
XM_011532799.1:c.1509A>C (MSH6)	XP_011531101.1:p.Ser503=
XM_011532800.1:c.1509A>C (MSH6)	XP_011531102.1:p.Ser503=
XM_024452819.1:c.1806A>C (MSH6)	XP_024308587.1:p.Ser602=
XM_024452820.1:c.1623A>C (MSH6)	XP_024308588.1:p.Ser541=
XM_024452821.1:c.1509A>C (MSH6)	XP_024308589.1:p.Ser503=
XM_024452822.1:c.900A>C (MSH6)	XP_024308590.1:p.Ser300=
NM_000179.3:c.1806A>C (MSH6) MANE Select	NP_000170.1:p.Ser602=
NM_001281492.2:c.1416A>C (MSH6)	NP_001268421.1:p.Ser472=
NM_001281493.2:c.900A>C (MSH6)	NP_001268422.1:p.Ser300=
NM_001281494.2:c.900A>C (MSH6)	NP_001268423.1:p.Ser300=