Canonical Allele Identifier: CA445159718

Gene: MSH3

Linked Data

• MyVariant Identifiers: chr5:g.79970851A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80675032A>T , CM000667.2:g.80675032A>T	GRCh38
NC_000005.9:g.79970851A>T , CM000667.1:g.79970851A>T	GRCh37
NC_000005.8:g.80006607A>T	NCBI36
NG_016607.1:g.25558A>T
NG_016607.2:g.25558A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.1077A>T MANE Select	ENSP00000265081.6:p.Ile359=
ENST00000658259.1:c.909A>T	ENSP00000499617.1:p.Ile303=
ENST00000667069.1:c.1077A>T	ENSP00000499502.1:p.Ile359=
ENST00000670357.1:c.1077A>T	ENSP00000499791.1:p.Ile359=
ENST00000265081.6:c.1077A>T	ENSP00000265081.6:p.Ile359=
NM_002439.4:c.1077A>T	NP_002430.3:p.Ile359=
NM_002439.5:c.1077A>T MANE Select	NP_002430.3:p.Ile359=