Canonical Allele Identifier: CA1558563994
Gene: MSH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873034T= , CM000667.2:g.80873034T= GRCh38
NC_000005.9:g.80168853T= , CM000667.1:g.80168853T= GRCh37
NC_000005.8:g.80204609T= NCBI36
NG_016607.1:g.223560T=
NG_016607.2:g.223560T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3131-82T= MANE Select ENSP00000265081.6:n.3131-82T=
ENST00000658259.1:c.2963-82T= ENSP00000499617.1:n.2963-82T=
ENST00000659302.1:c.539-82T=
ENST00000667069.1:c.2936-82T= ENSP00000499502.1:n.2936-82T=
ENST00000670357.1:c.*455-82T= ENSP00000499791.1:n.*455-82T=
ENST00000265081.6:c.3131-82T= ENSP00000265081.6:n.3131-82T=
NM_002439.4:c.3131-82T= NP_002430.3:n.3131-82T=
NM_002439.5:c.3131-82T= MANE Select NP_002430.3:n.3131-82T=