Canonical Allele Identifier: CA2674441070

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654884_80654899del , CM000667.2:g.80654884_80654899del	GRCh38
NC_000005.9:g.79950703_79950718del , CM000667.1:g.79950703_79950718del	GRCh37
NC_000005.8:g.79986459_79986474del	NCBI36
NG_016607.1:g.5410_5425del
NG_023304.1:g.5083_5098del
NG_016607.2:g.5410_5425del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-410_-395del (DHFR) MANE Select	NP_000782.1:n.-410_-395del
NM_002439.5:c.157_172del (MSH3) MANE Select	NP_002430.3:p.Ala53GlnfsTer22
ENST00000265081.7:c.157_172del (MSH3) MANE Select	ENSP00000265081.6:p.Ala53GlnfsTer22
ENST00000439211.7:c.-410_-395del (DHFR) MANE Select	ENSP00000396308.2:n.-410_-395del
NM_000791.3:c.-410_-395del (DHFR)	NP_000782.1:n.-410_-395del
NM_001290354.1:c.-516_-501del (DHFR)	NP_001277283.1:n.-516_-501del
NM_001290354.2:c.-516_-501del (DHFR)	NP_001277283.1:n.-516_-501del
NM_001290357.1:c.-410_-395del (DHFR)	NP_001277286.1:n.-410_-395del
NM_001290357.2:c.-410_-395del (DHFR)	NP_001277286.1:n.-410_-395del
NM_002439.4:c.157_172del (MSH3)	NP_002430.3:p.Ala53GlnfsTer22
NR_110936.1:n.83_98del (DHFR)
NR_110936.2:n.85_100del (DHFR)
ENST00000265081.6:c.157_172del (MSH3)	ENSP00000265081.6:p.Ala53GlnfsTer22
ENST00000439211.6:c.-410_-395del (DHFR)	ENSP00000396308.2:n.-410_-395del
ENST00000667069.1:c.157_172del (MSH3)	ENSP00000499502.1:p.Ala53GlnfsTer22
ENST00000670357.1:c.157_172del (MSH3)	ENSP00000499791.1:p.Ala53GlnfsTer22