Canonical Allele Identifier: CA2838196986
Gene: MSH4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.75883919A>T , CM000663.2:g.75883919A>T GRCh38
NC_000001.10:g.76349604A>T , CM000663.1:g.76349604A>T GRCh37
NC_000001.9:g.76122192A>T NCBI36
NG_029861.1:g.92049A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263187.4:c.2107+98A>T MANE Select ENSP00000263187.3:n.2107+98A>T
ENST00000263187.3:c.2107+98A>T ENSP00000263187.3:n.2107+98A>T
NM_002440.3:c.2107+98A>T NP_002431.2:n.2107+98A>T
NM_002440.4:c.2107+98A>T MANE Select NP_002431.2:n.2107+98A>T
Search 100 bp 5'
Search 100 bp 3'