Canonical Allele Identifier: CA1558440141

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654883_80654900delinsAGCGGCTGCAGCGGCCGC , CM000667.2:g.80654883_80654900delinsAGCGGCTGCAGCGGCCGC	GRCh38
NC_000005.9:g.79950702_79950719delinsAGCGGCTGCAGCGGCCGC , CM000667.1:g.79950702_79950719delinsAGCGGCTGCAGCGGCCGC	GRCh37
NC_000005.8:g.79986458_79986475delinsAGCGGCTGCAGCGGCCGC	NCBI36
NG_016607.1:g.5409_5426delinsAGCGGCTGCAGCGGCCGC
NG_023304.1:g.5082_5099delinsGCGGCCGCTGCAGCCGCT
NG_016607.2:g.5409_5426delinsAGCGGCTGCAGCGGCCGC

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-411_-394delinsGCGGCCGCTGCAGCCGCT (DHFR) MANE Select	NP_000782.1:n.-411_-394delinsGCGGCCGCTGCAGCCGCT
NM_002439.5:c.156_173delinsAGCGGCTGCAGCGGCCGC (MSH3) MANE Select	NP_002430.3:p.Ala52=
ENST00000265081.7:c.156_173delinsAGCGGCTGCAGCGGCCGC (MSH3) MANE Select	ENSP00000265081.6:p.Ala52=
ENST00000439211.7:c.-411_-394delinsGCGGCCGCTGCAGCCGCT (DHFR) MANE Select	ENSP00000396308.2:n.-411_-394delinsGCGGCCGCTGCAGCCGCT
NM_000791.3:c.-411_-394delinsGCGGCCGCTGCAGCCGCT (DHFR)	NP_000782.1:n.-411_-394delinsGCGGCCGCTGCAGCCGCT
NM_001290354.1:c.-517_-500delinsGCGGCCGCTGCAGCCGCT (DHFR)	NP_001277283.1:n.-517_-500delinsGCGGCCGCTGCAGCCGCT
NM_001290354.2:c.-517_-500delinsGCGGCCGCTGCAGCCGCT (DHFR)	NP_001277283.1:n.-517_-500delinsGCGGCCGCTGCAGCCGCT
NM_001290357.1:c.-411_-394delinsGCGGCCGCTGCAGCCGCT (DHFR)	NP_001277286.1:n.-411_-394delinsGCGGCCGCTGCAGCCGCT
NM_001290357.2:c.-411_-394delinsGCGGCCGCTGCAGCCGCT (DHFR)	NP_001277286.1:n.-411_-394delinsGCGGCCGCTGCAGCCGCT
NM_002439.4:c.156_173delinsAGCGGCTGCAGCGGCCGC (MSH3)	NP_002430.3:p.Ala52=
NR_110936.1:n.82_99delinsGCGGCCGCTGCAGCCGCT (DHFR)
NR_110936.2:n.84_101delinsGCGGCCGCTGCAGCCGCT (DHFR)
ENST00000265081.6:c.156_173delinsAGCGGCTGCAGCGGCCGC (MSH3)	ENSP00000265081.6:p.Ala52=
ENST00000439211.6:c.-411_-394delinsGCGGCCGCTGCAGCCGCT (DHFR)	ENSP00000396308.2:n.-411_-394delinsGCGGCCGCTGCAGCCGCT
ENST00000667069.1:c.156_173delinsAGCGGCTGCAGCGGCCGC (MSH3)	ENSP00000499502.1:p.Ala52=
ENST00000670357.1:c.156_173delinsAGCGGCTGCAGCGGCCGC (MSH3)	ENSP00000499791.1:p.Ala52=