Canonical Allele Identifier: CA1558563959
Gene: MSH3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80873019G= , CM000667.2:g.80873019G= GRCh38
NC_000005.9:g.80168838G= , CM000667.1:g.80168838G= GRCh37
NC_000005.8:g.80204594G= NCBI36
NG_016607.1:g.223545G=
NG_016607.2:g.223545G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.3131-97G= MANE Select ENSP00000265081.6:n.3131-97G=
ENST00000658259.1:c.2963-97G= ENSP00000499617.1:n.2963-97G=
ENST00000659302.1:c.539-97G=
ENST00000667069.1:c.2936-97G= ENSP00000499502.1:n.2936-97G=
ENST00000670357.1:c.*455-97G= ENSP00000499791.1:n.*455-97G=
ENST00000265081.6:c.3131-97G= ENSP00000265081.6:n.3131-97G=
NM_002439.4:c.3131-97G= NP_002430.3:n.3131-97G=
NM_002439.5:c.3131-97G= MANE Select NP_002430.3:n.3131-97G=