Canonical Allele Identifier: CA2709329485

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654861_80654887del , CM000667.2:g.80654861_80654887del	GRCh38
NC_000005.9:g.79950680_79950706del , CM000667.1:g.79950680_79950706del	GRCh37
NC_000005.8:g.79986436_79986462del	NCBI36
NG_016607.1:g.5387_5413del
NG_023304.1:g.5096_5122del
NG_016607.2:g.5387_5413del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-397_-371del (DHFR) MANE Select	NP_000782.1:n.-397_-371del
NM_002439.5:c.134_160del (MSH3) MANE Select	NP_002430.3:p.Asp45_Ala53del
ENST00000265081.7:c.134_160del (MSH3) MANE Select	ENSP00000265081.6:p.Asp45_Ala53del
ENST00000439211.7:c.-397_-371del (DHFR) MANE Select	ENSP00000396308.2:n.-397_-371del
NM_000791.3:c.-397_-371del (DHFR)	NP_000782.1:n.-397_-371del
NM_001290354.1:c.-503_-477del (DHFR)	NP_001277283.1:n.-503_-477del
NM_001290354.2:c.-503_-477del (DHFR)	NP_001277283.1:n.-503_-477del
NM_001290357.1:c.-397_-371del (DHFR)	NP_001277286.1:n.-397_-371del
NM_001290357.2:c.-397_-371del (DHFR)	NP_001277286.1:n.-397_-371del
NM_002439.4:c.134_160del (MSH3)	NP_002430.3:p.Asp45_Ala53del
NR_110936.1:n.96_122del (DHFR)
NR_110936.2:n.98_124del (DHFR)
ENST00000265081.6:c.134_160del (MSH3)	ENSP00000265081.6:p.Asp45_Ala53del
ENST00000439211.6:c.-397_-371del (DHFR)	ENSP00000396308.2:n.-397_-371del
ENST00000667069.1:c.134_160del (MSH3)	ENSP00000499502.1:p.Asp45_Ala53del
ENST00000670357.1:c.134_160del (MSH3)	ENSP00000499791.1:p.Asp45_Ala53del