Canonical Allele Identifier: CA426120978

Linked Data

ClinVar Variation Id: 2024947
ClinVar RCV Id: RCV002880408
MyVariant Identifiers: chr2:g.48026832A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.47799693A>C , CM000664.2:g.47799693A>C GRCh38
NC_000002.11:g.48026832A>C , CM000664.1:g.48026832A>C GRCh37
NC_000002.10:g.47880336A>C NCBI36
NG_007111.1:g.21547A>C , LRG_219:g.21547A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000411819.2:c.1413A>C (MSH6) ENSP00000406248.2:p.Ile471=
ENST00000420813.6:c.1413A>C (MSH6) ENSP00000390382.2:p.Ile471=
ENST00000455383.6:c.1413A>C (MSH6) ENSP00000397484.2:p.Ile471=
ENST00000700004.2:c.1710A>C (MSH6) ENSP00000514752.2:p.Ile570=
ENST00000699999.1:n.1794A>C (MSH6)
ENST00000700000.1:c.1606+104A>C (MSH6) ENSP00000514749.1:n.1606+104A>C
ENST00000700002.1:c.1716A>C (MSH6) ENSP00000514750.1:p.Ile572=
ENST00000700003.1:c.627+3630A>C (MSH6) ENSP00000514751.1:n.627+3630A>C
ENST00000700004.1:c.867A>C (MSH6) ENSP00000514752.1:p.Ile289=
ENST00000234420.11:c.1710A>C (MSH6) MANE Select ENSP00000234420.5:p.Ile570=
ENST00000540021.6:c.1320A>C (MSH6) ENSP00000446475.1:p.Ile440=
ENST00000652107.1:c.1413A>C (MSH6) ENSP00000498629.1:p.Ile471=
ENST00000673637.1:c.1413A>C (MSH6) ENSP00000501310.1:p.Ile471=
ENST00000234420.9:c.1710A>C (MSH6) ENSP00000234420.4:p.Ile570=
ENST00000405808.5:c.169+8502T>G (FBXO11) ENSP00000385127.1:n.169+8502T>G
ENST00000434234.5:c.*124+8301T>G (FBXO11) ENSP00000402692.1:n.*124+8301T>G
ENST00000445503.5:c.*1057A>C (MSH6) ENSP00000405294.1:n.*1057A>C
ENST00000538136.1:c.804A>C (MSH6) ENSP00000438580.1:p.Ile268=
ENST00000540021.5:c.1320A>C (MSH6) ENSP00000446475.1:p.Ile440=
ENST00000614496.4:c.804A>C (MSH6) ENSP00000477844.1:p.Ile268=
ENST00000616033.4:c.1707A>C (MSH6) ENSP00000480261.1:p.Ile569=
ENST00000622629.4:c.-1387A>C (MSH6) ENSP00000482078.1:n.-1387A>C
NM_000179.2:c.1710A>C , LRG_219t1:c.1710A>C (MSH6) NP_000170.1:p.Ile570=
NM_001281492.1:c.1320A>C (MSH6) NP_001268421.1:p.Ile440=
NM_001281493.1:c.804A>C (MSH6) NP_001268422.1:p.Ile268=
NM_001281494.1:c.804A>C (MSH6) NP_001268423.1:p.Ile268=
XM_005264271.1:c.1413A>C (MSH6) XP_005264328.1:p.Ile471=
XM_011532798.1:c.1527A>C (MSH6) XP_011531100.1:p.Ile509=
XM_011532799.1:c.1413A>C (MSH6) XP_011531101.1:p.Ile471=
XM_011532800.1:c.1413A>C (MSH6) XP_011531102.1:p.Ile471=
XM_024452819.1:c.1710A>C (MSH6) XP_024308587.1:p.Ile570=
XM_024452820.1:c.1527A>C (MSH6) XP_024308588.1:p.Ile509=
XM_024452821.1:c.1413A>C (MSH6) XP_024308589.1:p.Ile471=
XM_024452822.1:c.804A>C (MSH6) XP_024308590.1:p.Ile268=
NM_000179.3:c.1710A>C (MSH6) MANE Select NP_000170.1:p.Ile570=
NM_001281492.2:c.1320A>C (MSH6) NP_001268421.1:p.Ile440=
NM_001281493.2:c.804A>C (MSH6) NP_001268422.1:p.Ile268=
NM_001281494.2:c.804A>C (MSH6) NP_001268423.1:p.Ile268=