Canonical Allele Identifier: CA2496048839

Gene: MSH6 FBXO11

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47799597_47799598delinsTC , CM000664.2:g.47799597_47799598delinsTC	GRCh38
NC_000002.11:g.48026736_48026737delinsTC , CM000664.1:g.48026736_48026737delinsTC	GRCh37
NC_000002.10:g.47880240_47880241delinsTC	NCBI36
NG_007111.1:g.21451_21452delinsTC , LRG_219:g.21451_21452delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000411819.2:c.1317_1318delinsTC (MSH6)	ENSP00000406248.2:p.Tyr439=
ENST00000420813.6:c.1317_1318delinsTC (MSH6)	ENSP00000390382.2:p.Tyr439=
ENST00000455383.6:c.1317_1318delinsTC (MSH6)	ENSP00000397484.2:p.Tyr439=
ENST00000700004.2:c.1614_1615delinsTC (MSH6)	ENSP00000514752.2:p.Tyr538=
ENST00000699999.1:n.1698_1699delinsTC (MSH6)
ENST00000700000.1:c.1606+8_1606+9delinsTC (MSH6)	ENSP00000514749.1:n.1606+8_1606+9delinsTC...
ENST00000700002.1:c.1620_1621delinsTC (MSH6)	ENSP00000514750.1:p.Tyr540=
ENST00000700003.1:c.627+3534_627+3535delinsTC (MSH6)	ENSP00000514751.1:n.627+3534_627+3535deli...
ENST00000700004.1:c.771_772delinsTC (MSH6)	ENSP00000514752.1:p.Tyr257=
ENST00000234420.11:c.1614_1615delinsTC (MSH6) MANE Select	ENSP00000234420.5:p.Tyr538=
ENST00000540021.6:c.1224_1225delinsTC (MSH6)	ENSP00000446475.1:p.Tyr408=
ENST00000652107.1:c.1317_1318delinsTC (MSH6)	ENSP00000498629.1:p.Tyr439=
ENST00000673637.1:c.1317_1318delinsTC (MSH6)	ENSP00000501310.1:p.Tyr439=
ENST00000234420.9:c.1614_1615delinsTC (MSH6)	ENSP00000234420.4:p.Tyr538=
ENST00000405808.5:c.169+8597_169+8598delinsGA (FBXO11)	ENSP00000385127.1:n.169+8597_169+8598deli...
ENST00000434234.5:c.*124+8396_*124+8397delinsGA (FBXO11)	ENSP00000402692.1:n.*124+8396_*124+8397de...
ENST00000445503.5:c.*961_*962delinsTC (MSH6)	ENSP00000405294.1:n.*961_*962delinsTC
ENST00000538136.1:c.708_709delinsTC (MSH6)	ENSP00000438580.1:p.Tyr236=
ENST00000540021.5:c.1224_1225delinsTC (MSH6)	ENSP00000446475.1:p.Tyr408=
ENST00000614496.4:c.708_709delinsTC (MSH6)	ENSP00000477844.1:p.Tyr236=
ENST00000616033.4:c.1611_1612delinsTC (MSH6)	ENSP00000480261.1:p.Tyr537=
ENST00000622629.4:c.-1483_-1482delinsTC (MSH6)	ENSP00000482078.1:n.-1483_-1482delinsTC
NM_000179.2:c.1614_1615delinsTC , LRG_219t1:c.1614_1615delinsTC (MSH6)	NP_000170.1:p.Tyr538=
NM_001281492.1:c.1224_1225delinsTC (MSH6)	NP_001268421.1:p.Tyr408=
NM_001281493.1:c.708_709delinsTC (MSH6)	NP_001268422.1:p.Tyr236=
NM_001281494.1:c.708_709delinsTC (MSH6)	NP_001268423.1:p.Tyr236=
XM_005264271.1:c.1317_1318delinsTC (MSH6)	XP_005264328.1:p.Tyr439=
XM_011532798.1:c.1431_1432delinsTC (MSH6)	XP_011531100.1:p.Tyr477=
XM_011532799.1:c.1317_1318delinsTC (MSH6)	XP_011531101.1:p.Tyr439=
XM_011532800.1:c.1317_1318delinsTC (MSH6)	XP_011531102.1:p.Tyr439=
XM_024452819.1:c.1614_1615delinsTC (MSH6)	XP_024308587.1:p.Tyr538=
XM_024452820.1:c.1431_1432delinsTC (MSH6)	XP_024308588.1:p.Tyr477=
XM_024452821.1:c.1317_1318delinsTC (MSH6)	XP_024308589.1:p.Tyr439=
XM_024452822.1:c.708_709delinsTC (MSH6)	XP_024308590.1:p.Tyr236=
NM_000179.3:c.1614_1615delinsTC (MSH6) MANE Select	NP_000170.1:p.Tyr538=
NM_001281492.2:c.1224_1225delinsTC (MSH6)	NP_001268421.1:p.Tyr408=
NM_001281493.2:c.708_709delinsTC (MSH6)	NP_001268422.1:p.Tyr236=
NM_001281494.2:c.708_709delinsTC (MSH6)	NP_001268423.1:p.Tyr236=