Canonical Allele Identifier: CA2495872644

Gene: MSH2

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47475306_47475311delinsCGTTTT , CM000664.2:g.47475306_47475311delinsCGTTTT	GRCh38
NC_000002.11:g.47702445_47702450delinsCGTTTT , CM000664.1:g.47702445_47702450delinsCGTTTT	GRCh37
NC_000002.10:g.47555949_47555954delinsCGTTTT	NCBI36
NG_007110.2:g.77183_77188delinsCGTTTT , LRG_218:g.77183_77188delinsCGTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000644900.2:c.2005+36_2005+41delinsCGTTTT	ENSP00000495641.2:n.2005+36_2005+41delinsCGTTTT
ENST00000233146.7:c.2005+36_2005+41delinsCGTTTT MANE Select	ENSP00000233146.2:n.2005+36_2005+41delinsCGTTTT
ENST00000543555.6:c.1807+36_1807+41delinsCGTTTT	ENSP00000442697.1:n.1807+36_1807+41delinsCGTTTT
ENST00000644092.1:c.*305+36_*305+41delinsCGTTTT	ENSP00000496351.1:n.*305+36_*305+41delinsCGTTTT
ENST00000645339.1:c.2005+36_2005+41delinsCGTTTT	ENSP00000496441.1:n.2005+36_2005+41delinsCGTTTT
ENST00000645506.1:c.2005+36_2005+41delinsCGTTTT	ENSP00000495455.1:n.2005+36_2005+41delinsCGTTTT
ENST00000646415.1:c.2005+36_2005+41delinsCGTTTT	ENSP00000495543.1:n.2005+36_2005+41delinsCGTTTT
ENST00000233146.6:c.2005+36_2005+41delinsCGTTTT	ENSP00000233146.2:n.2005+36_2005+41delinsCGTTTT
ENST00000406134.5:c.2005+36_2005+41delinsCGTTTT	ENSP00000384199.1:n.2005+36_2005+41delinsCGTTTT
ENST00000543555.5:c.1807+36_1807+41delinsCGTTTT	ENSP00000442697.1:n.1807+36_1807+41delinsCGTTTT
ENST00000610696.4:c.*401+36_*401+41delinsCGTTTT	ENSP00000483159.1:n.*401+36_*401+41delinsCGTTTT
ENST00000613514.4:c.*545+36_*545+41delinsCGTTTT	ENSP00000484137.1:n.*545+36_*545+41delinsCGTTTT
ENST00000617333.3:c.*771+36_*771+41delinsCGTTTT	ENSP00000482468.1:n.*771+36_*771+41delinsCGTTTT
ENST00000617938.4:c.*977+36_*977+41delinsCGTTTT	ENSP00000481158.1:n.*977+36_*977+41delinsCGTTTT
ENST00000621359.2:c.2005+36_2005+41delinsCGTTTT	ENSP00000481416.1:n.2005+36_2005+41delinsCGTTTT
NM_000251.2:c.2005+36_2005+41delinsCGTTTT , LRG_218t1:c.2005+36_2005+41delinsCGTTTT	NP_000242.1:n.2005+36_2005+41delinsCGTTTT
NM_001258281.1:c.1807+36_1807+41delinsCGTTTT	NP_001245210.1:n.1807+36_1807+41delinsCGTTTT
XM_005264332.2:c.2005+36_2005+41delinsCGTTTT	XP_005264389.2:n.2005+36_2005+41delinsCGTTTT
XM_011532867.1:c.2005+36_2005+41delinsCGTTTT	XP_011531169.1:n.2005+36_2005+41delinsCGTTTT
XR_939685.1:n.2077+36_2077+41delinsCGTTTT
XM_005264332.4:c.2005+36_2005+41delinsCGTTTT	XP_005264389.2:n.2005+36_2005+41delinsCGTTTT
XM_011532867.2:c.2005+36_2005+41delinsCGTTTT	XP_011531169.1:n.2005+36_2005+41delinsCGTTTT
XR_001738747.2:n.2067+36_2067+41delinsCGTTTT
XR_939685.2:n.2067+36_2067+41delinsCGTTTT
NM_000251.3:c.2005+36_2005+41delinsCGTTTT MANE Select	NP_000242.1:n.2005+36_2005+41delinsCGTTTT