Canonical Allele Identifier: CA1077975531

Gene: MSH3 DHFR

Linked Data

• dbSNP Id: rs1749209899
• gnomAD v3: 5-80654905-G-GCCGCGGCGC
• gnomAD v4: 5-80654905-G-GCCGCGGCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654909_80654910insGGCGCCCGC , CM000667.2:g.80654909_80654910insGGCGCCCGC	GRCh38
NC_000005.9:g.79950728_79950729insGGCGCCCGC , CM000667.1:g.79950728_79950729insGGCGCCCGC	GRCh37
NC_000005.8:g.79986484_79986485insGGCGCCCGC	NCBI36
NG_016607.1:g.5435_5436insGGCGCCCGC
NG_023304.1:g.5076_5077insGCGCCGCGG
NG_016607.2:g.5435_5436insGGCGCCCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.182_183insGGCGCCCGC (MSH3) MANE Select	ENSP00000265081.6:p.Ala61_Ala62insAlaProAla
ENST00000439211.7:c.-417_-416insGCGCCGCGG (DHFR) MANE Select	ENSP00000396308.2:n.-417_-416insGCGCCGCGG
ENST00000667069.1:c.182_183insGGCGCCCGC (MSH3)	ENSP00000499502.1:p.Ala61_Ala62insAlaProAla
ENST00000670357.1:c.182_183insGGCGCCCGC (MSH3)	ENSP00000499791.1:p.Ala61_Ala62insAlaProAla
ENST00000265081.6:c.182_183insGGCGCCCGC (MSH3)	ENSP00000265081.6:p.Ala61_Ala62insAlaProAla
ENST00000439211.6:c.-417_-416insGCGCCGCGG (DHFR)	ENSP00000396308.2:n.-417_-416insGCGCCGCGG
NM_000791.3:c.-417_-416insGCGCCGCGG (DHFR)	NP_000782.1:n.-417_-416insGCGCCGCGG
NM_001290354.1:c.-523_-522insGCGCCGCGG (DHFR)	NP_001277283.1:n.-523_-522insGCGCCGCGG
NM_001290357.1:c.-417_-416insGCGCCGCGG (DHFR)	NP_001277286.1:n.-417_-416insGCGCCGCGG
NM_002439.4:c.182_183insGGCGCCCGC (MSH3)	NP_002430.3:p.Ala61_Ala62insAlaProAla
NR_110936.1:n.76_77insGCGCCGCGG (DHFR)
NM_000791.4:c.-417_-416insGCGCCGCGG (DHFR) MANE Select	NP_000782.1:n.-417_-416insGCGCCGCGG
NM_002439.5:c.182_183insGGCGCCCGC (MSH3) MANE Select	NP_002430.3:p.Ala61_Ala62insAlaProAla
NM_001290354.2:c.-523_-522insGCGCCGCGG (DHFR)	NP_001277283.1:n.-523_-522insGCGCCGCGG
NM_001290357.2:c.-417_-416insGCGCCGCGG (DHFR)	NP_001277286.1:n.-417_-416insGCGCCGCGG
NR_110936.2:n.78_79insGCGCCGCGG (DHFR)