Canonical Allele Identifier: CA1558563979
Gene: MSH3 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873027A= , CM000667.2:g.80873027A= GRCh38
NC_000005.9:g.80168846A= , CM000667.1:g.80168846A= GRCh37
NC_000005.8:g.80204602A= NCBI36
NG_016607.1:g.223553A=
NG_016607.2:g.223553A=

Transcript Alleles

HGVS Amino-acid change
ENST00000265081.7:c.3131-89A= MANE Select ENSP00000265081.6:n.3131-89A=
ENST00000658259.1:c.2963-89A= ENSP00000499617.1:n.2963-89A=
ENST00000659302.1:c.539-89A=
ENST00000667069.1:c.2936-89A= ENSP00000499502.1:n.2936-89A=
ENST00000670357.1:c.*455-89A= ENSP00000499791.1:n.*455-89A=
ENST00000265081.6:c.3131-89A= ENSP00000265081.6:n.3131-89A=
NM_002439.4:c.3131-89A= NP_002430.3:n.3131-89A=
NM_002439.5:c.3131-89A= MANE Select NP_002430.3:n.3131-89A=
Search 100 bp 5'
Search 100 bp 3'