Canonical Allele Identifier: CA1558440122

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654880_80654898delinsTGCAGCGGCTGCAGCGGCC , CM000667.2:g.80654880_80654898delinsTGCAGCGGCTGCAGCGGCC	GRCh38
NC_000005.9:g.79950699_79950717delinsTGCAGCGGCTGCAGCGGCC , CM000667.1:g.79950699_79950717delinsTGCAGCGGCTGCAGCGGCC	GRCh37
NC_000005.8:g.79986455_79986473delinsTGCAGCGGCTGCAGCGGCC	NCBI36
NG_016607.1:g.5406_5424delinsTGCAGCGGCTGCAGCGGCC
NG_023304.1:g.5084_5102delinsGGCCGCTGCAGCCGCTGCA
NG_016607.2:g.5406_5424delinsTGCAGCGGCTGCAGCGGCC

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-409_-391delinsGGCCGCTGCAGCCGCTGCA (DHFR) MANE Select	NP_000782.1:n.-409_-391delinsGGCCGCTGCAGCCGCTGCA
NM_002439.5:c.153_171delinsTGCAGCGGCTGCAGCGGCC (MSH3) MANE Select	NP_002430.3:p.Ala51=
ENST00000265081.7:c.153_171delinsTGCAGCGGCTGCAGCGGCC (MSH3) MANE Select	ENSP00000265081.6:p.Ala51=
ENST00000439211.7:c.-409_-391delinsGGCCGCTGCAGCCGCTGCA (DHFR) MANE Select	ENSP00000396308.2:n.-409_-391delinsGGCCGCTGCAGCCGCTGCA
NM_000791.3:c.-409_-391delinsGGCCGCTGCAGCCGCTGCA (DHFR)	NP_000782.1:n.-409_-391delinsGGCCGCTGCAGCCGCTGCA
NM_001290354.1:c.-515_-497delinsGGCCGCTGCAGCCGCTGCA (DHFR)	NP_001277283.1:n.-515_-497delinsGGCCGCTGCAGCCGCTGCA
NM_001290354.2:c.-515_-497delinsGGCCGCTGCAGCCGCTGCA (DHFR)	NP_001277283.1:n.-515_-497delinsGGCCGCTGCAGCCGCTGCA
NM_001290357.1:c.-409_-391delinsGGCCGCTGCAGCCGCTGCA (DHFR)	NP_001277286.1:n.-409_-391delinsGGCCGCTGCAGCCGCTGCA
NM_001290357.2:c.-409_-391delinsGGCCGCTGCAGCCGCTGCA (DHFR)	NP_001277286.1:n.-409_-391delinsGGCCGCTGCAGCCGCTGCA
NM_002439.4:c.153_171delinsTGCAGCGGCTGCAGCGGCC (MSH3)	NP_002430.3:p.Ala51=
NR_110936.1:n.84_102delinsGGCCGCTGCAGCCGCTGCA (DHFR)
NR_110936.2:n.86_104delinsGGCCGCTGCAGCCGCTGCA (DHFR)
ENST00000265081.6:c.153_171delinsTGCAGCGGCTGCAGCGGCC (MSH3)	ENSP00000265081.6:p.Ala51=
ENST00000439211.6:c.-409_-391delinsGGCCGCTGCAGCCGCTGCA (DHFR)	ENSP00000396308.2:n.-409_-391delinsGGCCGCTGCAGCCGCTGCA
ENST00000667069.1:c.153_171delinsTGCAGCGGCTGCAGCGGCC (MSH3)	ENSP00000499502.1:p.Ala51=
ENST00000670357.1:c.153_171delinsTGCAGCGGCTGCAGCGGCC (MSH3)	ENSP00000499791.1:p.Ala51=