Canonical Allele Identifier: CA2578350652

Gene: MSH3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80873029del , CM000667.2:g.80873029del	GRCh38
NC_000005.9:g.80168848del , CM000667.1:g.80168848del	GRCh37
NC_000005.8:g.80204604del	NCBI36
NG_016607.1:g.223555del
NG_016607.2:g.223555del

Transcript Alleles

HGVS	Amino-acid change
ENST00000265081.7:c.3131-87del MANE Select	ENSP00000265081.6:n.3131-87del
ENST00000658259.1:c.2963-87del	ENSP00000499617.1:n.2963-87del
ENST00000659302.1:c.539-87del
ENST00000667069.1:c.2936-87del	ENSP00000499502.1:n.2936-87del
ENST00000670357.1:c.*455-87del	ENSP00000499791.1:n.*455-87del
ENST00000265081.6:c.3131-87del	ENSP00000265081.6:n.3131-87del
NM_002439.4:c.3131-87del	NP_002430.3:n.3131-87del
NM_002439.5:c.3131-87del MANE Select	NP_002430.3:n.3131-87del