Canonical Allele Identifier: CA1030294378
Gene: MSH6 HGNC NCBI

Linked Data

dbSNP Id: rs1668101954
gnomAD v4: 2-47783160-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47783160A>G , CM000664.2:g.47783160A>G GRCh38
NC_000002.11:g.48010299A>G , CM000664.1:g.48010299A>G GRCh37
NC_000002.10:g.47863803A>G NCBI36
NG_007111.1:g.5014A>G , LRG_219:g.5014A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000700004.2:c.-74A>G ENSP00000514752.2:n.-74A>G
ENST00000699999.1:n.11A>G
ENST00000700000.1:c.-74A>G ENSP00000514749.1:n.-74A>G
ENST00000234420.11:c.-74A>G MANE Select ENSP00000234420.5:n.-74A>G
ENST00000652107.1:c.-37-7767A>G ENSP00000498629.1:n.-37-7767A>G
ENST00000673637.1:c.-109A>G ENSP00000501310.1:n.-109A>G
ENST00000673922.1:n.16A>G
ENST00000234420.9:c.-74A>G ENSP00000234420.4:n.-74A>G
ENST00000445503.5:c.-74A>G ENSP00000405294.1:n.-74A>G
ENST00000456246.1:c.-74A>G ENSP00000410570.1:n.-74A>G
ENST00000540021.5:c.-74A>G ENSP00000446475.1:n.-74A>G
ENST00000606499.1:c.-37-7767A>G ENSP00000475605.1:n.-37-7767A>G
ENST00000614496.4:c.-810A>G ENSP00000477844.1:n.-810A>G
ENST00000616033.4:c.-74A>G ENSP00000480261.1:n.-74A>G
ENST00000622629.4:c.-3170A>G ENSP00000482078.1:n.-3170A>G
NM_000179.2:c.-74A>G , LRG_219t1:c.-74A>G NP_000170.1:n.-74A>G
NM_001281492.1:c.-74A>G NP_001268421.1:n.-74A>G
NM_001281493.1:c.-810A>G NP_001268422.1:n.-810A>G
XM_011532800.1:c.-109A>G XP_011531102.1:n.-109A>G
XM_024452819.1:c.-74A>G XP_024308587.1:n.-74A>G
NM_000179.3:c.-74A>G MANE Select NP_000170.1:n.-74A>G
NM_001281492.2:c.-74A>G NP_001268421.1:n.-74A>G
NM_001281493.2:c.-810A>G NP_001268422.1:n.-810A>G