Canonical Allele Identifier: CA2674441063

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654886_80654887insCCCCCAGCG , CM000667.2:g.80654886_80654887insCCCCCAGCG	GRCh38
NC_000005.9:g.79950705_79950706insCCCCCAGCG , CM000667.1:g.79950705_79950706insCCCCCAGCG	GRCh37
NC_000005.8:g.79986461_79986462insCCCCCAGCG	NCBI36
NG_016607.1:g.5412_5413insCCCCCAGCG
NG_023304.1:g.5100_5101insGGGGCGCTG
NG_016607.2:g.5412_5413insCCCCCAGCG

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-393_-392insGGGGCGCTG (DHFR) MANE Select	NP_000782.1:n.-393_-392insGGGGCGCTG
NM_002439.5:c.159_160insCCCCCAGCG (MSH3) MANE Select	NP_002430.3:p.Ala53_Ala54insProProAla
ENST00000265081.7:c.159_160insCCCCCAGCG (MSH3) MANE Select	ENSP00000265081.6:p.Ala53_Ala54insProProAla
ENST00000439211.7:c.-393_-392insGGGGCGCTG (DHFR) MANE Select	ENSP00000396308.2:n.-393_-392insGGGGCGCTG
NM_000791.3:c.-393_-392insGGGGCGCTG (DHFR)	NP_000782.1:n.-393_-392insGGGGCGCTG
NM_001290354.1:c.-499_-498insGGGGCGCTG (DHFR)	NP_001277283.1:n.-499_-498insGGGGCGCTG
NM_001290354.2:c.-499_-498insGGGGCGCTG (DHFR)	NP_001277283.1:n.-499_-498insGGGGCGCTG
NM_001290357.1:c.-393_-392insGGGGCGCTG (DHFR)	NP_001277286.1:n.-393_-392insGGGGCGCTG
NM_001290357.2:c.-393_-392insGGGGCGCTG (DHFR)	NP_001277286.1:n.-393_-392insGGGGCGCTG
NM_002439.4:c.159_160insCCCCCAGCG (MSH3)	NP_002430.3:p.Ala53_Ala54insProProAla
NR_110936.1:n.100_101insGGGGCGCTG (DHFR)
NR_110936.2:n.102_103insGGGGCGCTG (DHFR)
ENST00000265081.6:c.159_160insCCCCCAGCG (MSH3)	ENSP00000265081.6:p.Ala53_Ala54insProProAla
ENST00000439211.6:c.-393_-392insGGGGCGCTG (DHFR)	ENSP00000396308.2:n.-393_-392insGGGGCGCTG
ENST00000667069.1:c.159_160insCCCCCAGCG (MSH3)	ENSP00000499502.1:p.Ala53_Ala54insProProAla
ENST00000670357.1:c.159_160insCCCCCAGCG (MSH3)	ENSP00000499791.1:p.Ala53_Ala54insProProAla