Canonical Allele Identifier: CA3246845632

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654880_80654894del , CM000667.2:g.80654880_80654894del	GRCh38
NC_000005.9:g.79950699_79950713del , CM000667.1:g.79950699_79950713del	GRCh37
NC_000005.8:g.79986455_79986469del	NCBI36
NG_016607.1:g.5406_5420del
NG_023304.1:g.5090_5104del
NG_016607.2:g.5406_5420del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-403_-389del (DHFR) MANE Select	NP_000782.1:n.-403_-389del
NM_002439.5:c.153_167del (MSH3) MANE Select	NP_002430.3:p.Ala52_Ala56del
ENST00000265081.7:c.153_167del (MSH3) MANE Select	ENSP00000265081.6:p.Ala52_Ala56del
ENST00000439211.7:c.-403_-389del (DHFR) MANE Select	ENSP00000396308.2:n.-403_-389del
NM_000791.3:c.-403_-389del (DHFR)	NP_000782.1:n.-403_-389del
NM_001290354.1:c.-509_-495del (DHFR)	NP_001277283.1:n.-509_-495del
NM_001290354.2:c.-509_-495del (DHFR)	NP_001277283.1:n.-509_-495del
NM_001290357.1:c.-403_-389del (DHFR)	NP_001277286.1:n.-403_-389del
NM_001290357.2:c.-403_-389del (DHFR)	NP_001277286.1:n.-403_-389del
NM_002439.4:c.153_167del (MSH3)	NP_002430.3:p.Ala52_Ala56del
NR_110936.1:n.90_104del (DHFR)
NR_110936.2:n.92_106del (DHFR)
ENST00000265081.6:c.153_167del (MSH3)	ENSP00000265081.6:p.Ala52_Ala56del
ENST00000439211.6:c.-403_-389del (DHFR)	ENSP00000396308.2:n.-403_-389del
ENST00000667069.1:c.153_167del (MSH3)	ENSP00000499502.1:p.Ala52_Ala56del
ENST00000670357.1:c.153_167del (MSH3)	ENSP00000499791.1:p.Ala52_Ala56del