Canonical Allele Identifier: CA2674441401

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654930_80654931insGCCGCCAGC , CM000667.2:g.80654930_80654931insGCCGCCAGC	GRCh38
NC_000005.9:g.79950749_79950750insGCCGCCAGC , CM000667.1:g.79950749_79950750insGCCGCCAGC	GRCh37
NC_000005.8:g.79986505_79986506insGCCGCCAGC	NCBI36
NG_016607.1:g.5456_5457insGCCGCCAGC
NG_023304.1:g.5056_5057insCGGCGCTGG
NG_016607.2:g.5456_5457insGCCGCCAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.203_204insGCCGCCAGC (MSH3) MANE Select	ENSP00000265081.6:p.Ala68_Pro69insProProAla
ENST00000439211.7:c.-437_-436insCGGCGCTGG (DHFR) MANE Select	ENSP00000396308.2:n.-437_-436insCGGCGCTGG
ENST00000667069.1:c.203_204insGCCGCCAGC (MSH3)	ENSP00000499502.1:p.Ala68_Pro69insProProAla
ENST00000670357.1:c.203_204insGCCGCCAGC (MSH3)	ENSP00000499791.1:p.Ala68_Pro69insProProAla
ENST00000265081.6:c.203_204insGCCGCCAGC (MSH3)	ENSP00000265081.6:p.Ala68_Pro69insProProAla
ENST00000439211.6:c.-437_-436insCGGCGCTGG (DHFR)	ENSP00000396308.2:n.-437_-436insCGGCGCTGG
NM_000791.3:c.-437_-436insCGGCGCTGG (DHFR)	NP_000782.1:n.-437_-436insCGGCGCTGG
NM_001290354.1:c.-543_-542insCGGCGCTGG (DHFR)	NP_001277283.1:n.-543_-542insCGGCGCTGG
NM_001290357.1:c.-437_-436insCGGCGCTGG (DHFR)	NP_001277286.1:n.-437_-436insCGGCGCTGG
NM_002439.4:c.203_204insGCCGCCAGC (MSH3)	NP_002430.3:p.Ala68_Pro69insProProAla
NR_110936.1:n.56_57insCGGCGCTGG (DHFR)
NM_000791.4:c.-437_-436insCGGCGCTGG (DHFR) MANE Select	NP_000782.1:n.-437_-436insCGGCGCTGG
NM_002439.5:c.203_204insGCCGCCAGC (MSH3) MANE Select	NP_002430.3:p.Ala68_Pro69insProProAla
NM_001290354.2:c.-543_-542insCGGCGCTGG (DHFR)	NP_001277283.1:n.-543_-542insCGGCGCTGG
NM_001290357.2:c.-437_-436insCGGCGCTGG (DHFR)	NP_001277286.1:n.-437_-436insCGGCGCTGG
NR_110936.2:n.58_59insCGGCGCTGG (DHFR)