Canonical Allele Identifier: CA2674441069

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654884_80654891del , CM000667.2:g.80654884_80654891del	GRCh38
NC_000005.9:g.79950703_79950710del , CM000667.1:g.79950703_79950710del	GRCh37
NC_000005.8:g.79986459_79986466del	NCBI36
NG_016607.1:g.5410_5417del
NG_023304.1:g.5091_5098del
NG_016607.2:g.5410_5417del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-402_-395del (DHFR) MANE Select	NP_000782.1:n.-402_-395del
NM_002439.5:c.157_164del (MSH3) MANE Select	NP_002430.3:p.Ala53SerfsTer29
ENST00000265081.7:c.157_164del (MSH3) MANE Select	ENSP00000265081.6:p.Ala53SerfsTer29
ENST00000439211.7:c.-402_-395del (DHFR) MANE Select	ENSP00000396308.2:n.-402_-395del
NM_000791.3:c.-402_-395del (DHFR)	NP_000782.1:n.-402_-395del
NM_001290354.1:c.-508_-501del (DHFR)	NP_001277283.1:n.-508_-501del
NM_001290354.2:c.-508_-501del (DHFR)	NP_001277283.1:n.-508_-501del
NM_001290357.1:c.-402_-395del (DHFR)	NP_001277286.1:n.-402_-395del
NM_001290357.2:c.-402_-395del (DHFR)	NP_001277286.1:n.-402_-395del
NM_002439.4:c.157_164del (MSH3)	NP_002430.3:p.Ala53SerfsTer29
NR_110936.1:n.91_98del (DHFR)
NR_110936.2:n.93_100del (DHFR)
ENST00000265081.6:c.157_164del (MSH3)	ENSP00000265081.6:p.Ala53SerfsTer29
ENST00000439211.6:c.-402_-395del (DHFR)	ENSP00000396308.2:n.-402_-395del
ENST00000667069.1:c.157_164del (MSH3)	ENSP00000499502.1:p.Ala53SerfsTer29
ENST00000670357.1:c.157_164del (MSH3)	ENSP00000499791.1:p.Ala53SerfsTer29