Canonical Allele Identifier: CA363349395

Gene: MSH5 MSH5-SAPCD1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31744026G>A , CM000668.2:g.31744026G>A	GRCh38
NC_000006.11:g.31711803G>A , CM000668.1:g.31711803G>A	GRCh37
NC_000006.10:g.31819782G>A	NCBI36
NG_011611.1:g.9030G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_172166.4:c.537+1G>A (MSH5) MANE Select	NP_751898.1:n.537+1G>A
ENST00000375750.9:c.537+1G>A (MSH5) MANE Select	ENSP00000364903.3:n.537+1G>A
NM_002441.4:c.537+1G>A (MSH5)	NP_002432.1:n.537+1G>A
NM_002441.5:c.537+1G>A (MSH5)	NP_002432.1:n.537+1G>A
NM_025259.5:c.537+1G>A (MSH5)	NP_079535.4:n.537+1G>A
NM_025259.6:c.537+1G>A (MSH5)	NP_079535.4:n.537+1G>A
NM_172165.3:c.537+1G>A (MSH5)	NP_751897.1:n.537+1G>A
NM_172165.4:c.537+1G>A (MSH5)	NP_751897.1:n.537+1G>A
NM_172166.3:c.537+1G>A (MSH5)	NP_751898.1:n.537+1G>A
NR_037846.1:n.665+1G>A (MSH5-SAPCD1)
ENST00000375703.7:c.537+1G>A (MSH5)	ENSP00000364855.3:n.537+1G>A
ENST00000375740.7:c.537+1G>A (MSH5)	ENSP00000364892.3:n.537+1G>A
ENST00000375750.7:c.537+1G>A (MSH5)	ENSP00000364903.3:n.537+1G>A
ENST00000375755.7:c.537+1G>A (MSH5)	ENSP00000364908.3:n.537+1G>A
ENST00000375755.8:c.537+1G>A (MSH5)	ENSP00000364908.3:n.537+1G>A
ENST00000423982.6:c.537+1G>A (MSH5)	ENSP00000406352.2:n.537+1G>A
ENST00000425703.5:c.537+1G>A (MSH5)	ENSP00000402842.1:n.537+1G>A
ENST00000450148.5:c.48+1G>A (MSH5)	ENSP00000394971.1:n.48+1G>A
ENST00000463144.5:c.307+1G>A (MSH5)
ENST00000482280.1:n.608+1G>A (MSH5)
ENST00000493662.6:c.537+1G>A (MSH5-SAPCD1)	ENSP00000417871.2:n.537+1G>A
ENST00000650702.1:n.762G>A (MSH5)