Canonical Allele Identifier: CA1619295560

Gene: MSH5 MSH5-SAPCD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31762148C= , CM000668.2:g.31762148C=	GRCh38
NC_000006.11:g.31729925C= , CM000668.1:g.31729925C=	GRCh37
NC_000006.10:g.31837904C=	NCBI36
NG_011611.1:g.27152C=

Transcript Alleles

HGVS	Amino-acid Change
NM_172166.4:c.2356C= (MSH5) MANE Select	NP_751898.1:p.Pro786=
ENST00000375750.9:c.2356C= (MSH5) MANE Select	ENSP00000364903.3:p.Pro786=
NM_002441.4:c.2356C= (MSH5)	NP_002432.1:p.Pro786=
NM_002441.5:c.2356C= (MSH5)	NP_002432.1:p.Pro786=
NM_025259.5:c.2320C= (MSH5)	NP_079535.4:p.Pro774=
NM_025259.6:c.2320C= (MSH5)	NP_079535.4:p.Pro774=
NM_172165.3:c.2359C= (MSH5)	NP_751897.1:p.Pro787=
NM_172165.4:c.2359C= (MSH5)	NP_751897.1:p.Pro787=
NM_172166.3:c.2356C= (MSH5)	NP_751898.1:p.Pro786=
NR_037846.1:n.2535C= (MSH5-SAPCD1)
ENST00000375703.7:c.2359C= (MSH5)	ENSP00000364855.3:p.Pro787=
ENST00000375740.7:c.2320C= (MSH5)	ENSP00000364892.3:p.Pro774=
ENST00000375750.7:c.2356C= (MSH5)	ENSP00000364903.3:p.Pro786=
ENST00000375755.7:c.2356C= (MSH5)	ENSP00000364908.3:p.Pro786=
ENST00000375755.8:c.2356C= (MSH5)	ENSP00000364908.3:p.Pro786=
ENST00000395853.5:c.1378C= (MSH5)	ENSP00000379194.1:p.Pro460=
ENST00000423982.6:c.*344C= (MSH5)	ENSP00000406352.2:n.*344C=
ENST00000429846.1:c.322C= (MSH5)	ENSP00000406849.1:p.Pro108=
ENST00000463144.5:c.2043C= (MSH5)
ENST00000484309.5:c.563C= (MSH5)	ENSP00000420232.1:n.563C=
ENST00000491552.1:n.424C= (MSH5-SAPCD1)
ENST00000493662.6:c.2407C= (MSH5-SAPCD1)	ENSP00000417871.2:p.Pro803=
ENST00000494458.1:n.226C= (MSH5)
ENST00000498473.6:c.907C= (MSH5-SAPCD1)
ENST00000650702.1:n.2783C= (MSH5)