Canonical Allele Identifier: CA425986945

Gene: MSH6

Linked Data

• ClinVar Variation Id: 825033
• ClinVar RCV Id: RCV001022766 ; RCV003594082
• dbSNP Id: rs1572697821
• MyVariant Identifiers: chr2:g.48010417G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47783278G>A , CM000664.2:g.47783278G>A	GRCh38
NC_000002.11:g.48010417G>A , CM000664.1:g.48010417G>A	GRCh37
NC_000002.10:g.47863921G>A	NCBI36
NG_007111.1:g.5132G>A , LRG_219:g.5132G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000700004.2:c.45G>A	ENSP00000514752.2:p.Pro15=
ENST00000699999.1:n.129G>A
ENST00000700000.1:c.45G>A	ENSP00000514749.1:p.Pro15=
ENST00000700001.1:n.117G>A
ENST00000700002.1:c.45G>A	ENSP00000514750.1:p.Pro15=
ENST00000700003.1:c.45G>A	ENSP00000514751.1:p.Pro15=
ENST00000234420.11:c.45G>A MANE Select	ENSP00000234420.5:p.Pro15=
ENST00000540021.6:c.45G>A	ENSP00000446475.1:p.Pro15=
ENST00000652107.1:c.-37-7649G>A	ENSP00000498629.1:n.-37-7649G>A
ENST00000673637.1:c.-38+47G>A	ENSP00000501310.1:n.-38+47G>A
ENST00000673922.1:n.134G>A
ENST00000234420.9:c.45G>A	ENSP00000234420.4:p.Pro15=
ENST00000445503.5:c.45G>A	ENSP00000405294.1:p.Pro15=
ENST00000456246.1:c.45G>A	ENSP00000410570.1:p.Pro15=
ENST00000493177.1:n.109G>A
ENST00000540021.5:c.45G>A	ENSP00000446475.1:p.Pro15=
ENST00000606499.1:c.-37-7649G>A	ENSP00000475605.1:n.-37-7649G>A
ENST00000614496.4:c.-692G>A	ENSP00000477844.1:n.-692G>A
ENST00000616033.4:c.45G>A	ENSP00000480261.1:p.Pro15=
ENST00000622629.4:c.-3052G>A	ENSP00000482078.1:n.-3052G>A
NM_000179.2:c.45G>A , LRG_219t1:c.45G>A	NP_000170.1:p.Pro15=
NM_001281492.1:c.45G>A	NP_001268421.1:p.Pro15=
NM_001281493.1:c.-692G>A	NP_001268422.1:n.-692G>A
XM_011532800.1:c.-38+47G>A	XP_011531102.1:n.-38+47G>A
XM_024452819.1:c.45G>A	XP_024308587.1:p.Pro15=
XM_024452822.1:c.-692G>A	XP_024308590.1:n.-692G>A
NM_000179.3:c.45G>A MANE Select	NP_000170.1:p.Pro15=
NM_001281492.2:c.45G>A	NP_001268421.1:p.Pro15=
NM_001281493.2:c.-692G>A	NP_001268422.1:n.-692G>A