Canonical Allele Identifier: CA2709118294

Gene: MSH3 DHFR

Linked Data

• dbSNP Id: rs1749209899

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654909_80654910insCGCGCCCGC , CM000667.2:g.80654909_80654910insCGCGCCCGC	GRCh38
NC_000005.9:g.79950728_79950729insCGCGCCCGC , CM000667.1:g.79950728_79950729insCGCGCCCGC	GRCh37
NC_000005.8:g.79986484_79986485insCGCGCCCGC	NCBI36
NG_016607.1:g.5435_5436insCGCGCCCGC
NG_023304.1:g.5076_5077insGCGCGGCGG
NG_016607.2:g.5435_5436insCGCGCCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.182_183insCGCGCCCGC (MSH3) MANE Select	ENSP00000265081.6:p.Ala61_Ala62insAlaProAla
ENST00000439211.7:c.-417_-416insGCGCGGCGG (DHFR) MANE Select	ENSP00000396308.2:n.-417_-416insGCGCGGCGG
ENST00000667069.1:c.182_183insCGCGCCCGC (MSH3)	ENSP00000499502.1:p.Ala61_Ala62insAlaProAla
ENST00000670357.1:c.182_183insCGCGCCCGC (MSH3)	ENSP00000499791.1:p.Ala61_Ala62insAlaProAla
ENST00000265081.6:c.182_183insCGCGCCCGC (MSH3)	ENSP00000265081.6:p.Ala61_Ala62insAlaProAla
ENST00000439211.6:c.-417_-416insGCGCGGCGG (DHFR)	ENSP00000396308.2:n.-417_-416insGCGCGGCGG
NM_000791.3:c.-417_-416insGCGCGGCGG (DHFR)	NP_000782.1:n.-417_-416insGCGCGGCGG
NM_001290354.1:c.-523_-522insGCGCGGCGG (DHFR)	NP_001277283.1:n.-523_-522insGCGCGGCGG
NM_001290357.1:c.-417_-416insGCGCGGCGG (DHFR)	NP_001277286.1:n.-417_-416insGCGCGGCGG
NM_002439.4:c.182_183insCGCGCCCGC (MSH3)	NP_002430.3:p.Ala61_Ala62insAlaProAla
NR_110936.1:n.76_77insGCGCGGCGG (DHFR)
NM_000791.4:c.-417_-416insGCGCGGCGG (DHFR) MANE Select	NP_000782.1:n.-417_-416insGCGCGGCGG
NM_002439.5:c.182_183insCGCGCCCGC (MSH3) MANE Select	NP_002430.3:p.Ala61_Ala62insAlaProAla
NM_001290354.2:c.-523_-522insGCGCGGCGG (DHFR)	NP_001277283.1:n.-523_-522insGCGCGGCGG
NM_001290357.2:c.-417_-416insGCGCGGCGG (DHFR)	NP_001277286.1:n.-417_-416insGCGCGGCGG
NR_110936.2:n.78_79insGCGCGGCGG (DHFR)