Canonical Allele Identifier: CA2709331945

Gene: MSH3 DHFR

Linked Data

• dbSNP Id: rs2112798074

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654912_80654913insCCCCGCAGC , CM000667.2:g.80654912_80654913insCCCCGCAGC	GRCh38
NC_000005.9:g.79950731_79950732insCCCCGCAGC , CM000667.1:g.79950731_79950732insCCCCGCAGC	GRCh37
NC_000005.8:g.79986487_79986488insCCCCGCAGC	NCBI36
NG_016607.1:g.5438_5439insCCCCGCAGC
NG_023304.1:g.5076_5077insGGGCTGCGG
NG_016607.2:g.5438_5439insCCCCGCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.185_186insCCCCGCAGC (MSH3) MANE Select	ENSP00000265081.6:p.Ala62_Pro63insProAlaAla
ENST00000439211.7:c.-417_-416insGGGCTGCGG (DHFR) MANE Select	ENSP00000396308.2:n.-417_-416insGGGCTGCGG
ENST00000667069.1:c.185_186insCCCCGCAGC (MSH3)	ENSP00000499502.1:p.Ala62_Pro63insProAlaAla
ENST00000670357.1:c.185_186insCCCCGCAGC (MSH3)	ENSP00000499791.1:p.Ala62_Pro63insProAlaAla
ENST00000265081.6:c.185_186insCCCCGCAGC (MSH3)	ENSP00000265081.6:p.Ala62_Pro63insProAlaAla
ENST00000439211.6:c.-417_-416insGGGCTGCGG (DHFR)	ENSP00000396308.2:n.-417_-416insGGGCTGCGG
NM_000791.3:c.-417_-416insGGGCTGCGG (DHFR)	NP_000782.1:n.-417_-416insGGGCTGCGG
NM_001290354.1:c.-523_-522insGGGCTGCGG (DHFR)	NP_001277283.1:n.-523_-522insGGGCTGCGG
NM_001290357.1:c.-417_-416insGGGCTGCGG (DHFR)	NP_001277286.1:n.-417_-416insGGGCTGCGG
NM_002439.4:c.185_186insCCCCGCAGC (MSH3)	NP_002430.3:p.Ala62_Pro63insProAlaAla
NR_110936.1:n.76_77insGGGCTGCGG (DHFR)
NM_000791.4:c.-417_-416insGGGCTGCGG (DHFR) MANE Select	NP_000782.1:n.-417_-416insGGGCTGCGG
NM_002439.5:c.185_186insCCCCGCAGC (MSH3) MANE Select	NP_002430.3:p.Ala62_Pro63insProAlaAla
NM_001290354.2:c.-523_-522insGGGCTGCGG (DHFR)	NP_001277283.1:n.-523_-522insGGGCTGCGG
NM_001290357.2:c.-417_-416insGGGCTGCGG (DHFR)	NP_001277286.1:n.-417_-416insGGGCTGCGG
NR_110936.2:n.78_79insGGGCTGCGG (DHFR)