Canonical Allele Identifier: CA2674441104

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654906_80654907insTGCAGCGGC , CM000667.2:g.80654906_80654907insTGCAGCGGC	GRCh38
NC_000005.9:g.79950725_79950726insTGCAGCGGC , CM000667.1:g.79950725_79950726insTGCAGCGGC	GRCh37
NC_000005.8:g.79986481_79986482insTGCAGCGGC	NCBI36
NG_016607.1:g.5432_5433insTGCAGCGGC
NG_023304.1:g.5083_5084insAGCCGCTGC
NG_016607.2:g.5432_5433insTGCAGCGGC

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-410_-409insAGCCGCTGC (DHFR) MANE Select	NP_000782.1:n.-410_-409insAGCCGCTGC
NM_002439.5:c.179_180insTGCAGCGGC (MSH3) MANE Select	NP_002430.3:p.Ala60_Ala61insAlaAlaAla
ENST00000265081.7:c.179_180insTGCAGCGGC (MSH3) MANE Select	ENSP00000265081.6:p.Ala60_Ala61insAlaAlaAla
ENST00000439211.7:c.-410_-409insAGCCGCTGC (DHFR) MANE Select	ENSP00000396308.2:n.-410_-409insAGCCGCTGC
NM_000791.3:c.-410_-409insAGCCGCTGC (DHFR)	NP_000782.1:n.-410_-409insAGCCGCTGC
NM_001290354.1:c.-516_-515insAGCCGCTGC (DHFR)	NP_001277283.1:n.-516_-515insAGCCGCTGC
NM_001290354.2:c.-516_-515insAGCCGCTGC (DHFR)	NP_001277283.1:n.-516_-515insAGCCGCTGC
NM_001290357.1:c.-410_-409insAGCCGCTGC (DHFR)	NP_001277286.1:n.-410_-409insAGCCGCTGC
NM_001290357.2:c.-410_-409insAGCCGCTGC (DHFR)	NP_001277286.1:n.-410_-409insAGCCGCTGC
NM_002439.4:c.179_180insTGCAGCGGC (MSH3)	NP_002430.3:p.Ala60_Ala61insAlaAlaAla
NR_110936.1:n.83_84insAGCCGCTGC (DHFR)
NR_110936.2:n.85_86insAGCCGCTGC (DHFR)
ENST00000265081.6:c.179_180insTGCAGCGGC (MSH3)	ENSP00000265081.6:p.Ala60_Ala61insAlaAlaAla
ENST00000439211.6:c.-410_-409insAGCCGCTGC (DHFR)	ENSP00000396308.2:n.-410_-409insAGCCGCTGC
ENST00000667069.1:c.179_180insTGCAGCGGC (MSH3)	ENSP00000499502.1:p.Ala60_Ala61insAlaAlaAla
ENST00000670357.1:c.179_180insTGCAGCGGC (MSH3)	ENSP00000499791.1:p.Ala60_Ala61insAlaAlaAla