Canonical Allele Identifier: CA2674441058

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654887_80654888insATGCAGCGG , CM000667.2:g.80654887_80654888insATGCAGCGG	GRCh38
NC_000005.9:g.79950706_79950707insATGCAGCGG , CM000667.1:g.79950706_79950707insATGCAGCGG	GRCh37
NC_000005.8:g.79986462_79986463insATGCAGCGG	NCBI36
NG_016607.1:g.5413_5414insATGCAGCGG
NG_023304.1:g.5102_5103insTCCGCTGCA
NG_016607.2:g.5413_5414insATGCAGCGG

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-391_-390insTCCGCTGCA (DHFR) MANE Select	NP_000782.1:n.-391_-390insTCCGCTGCA
NM_002439.5:c.160_161insATGCAGCGG (MSH3) MANE Select	NP_002430.3:p.Ala53_Ala54insAspAlaAla
ENST00000265081.7:c.160_161insATGCAGCGG (MSH3) MANE Select	ENSP00000265081.6:p.Ala53_Ala54insAspAlaAla
ENST00000439211.7:c.-391_-390insTCCGCTGCA (DHFR) MANE Select	ENSP00000396308.2:n.-391_-390insTCCGCTGCA
NM_000791.3:c.-391_-390insTCCGCTGCA (DHFR)	NP_000782.1:n.-391_-390insTCCGCTGCA
NM_001290354.1:c.-497_-496insTCCGCTGCA (DHFR)	NP_001277283.1:n.-497_-496insTCCGCTGCA
NM_001290354.2:c.-497_-496insTCCGCTGCA (DHFR)	NP_001277283.1:n.-497_-496insTCCGCTGCA
NM_001290357.1:c.-391_-390insTCCGCTGCA (DHFR)	NP_001277286.1:n.-391_-390insTCCGCTGCA
NM_001290357.2:c.-391_-390insTCCGCTGCA (DHFR)	NP_001277286.1:n.-391_-390insTCCGCTGCA
NM_002439.4:c.160_161insATGCAGCGG (MSH3)	NP_002430.3:p.Ala53_Ala54insAspAlaAla
NR_110936.1:n.102_103insTCCGCTGCA (DHFR)
NR_110936.2:n.104_105insTCCGCTGCA (DHFR)
ENST00000265081.6:c.160_161insATGCAGCGG (MSH3)	ENSP00000265081.6:p.Ala53_Ala54insAspAlaAla
ENST00000439211.6:c.-391_-390insTCCGCTGCA (DHFR)	ENSP00000396308.2:n.-391_-390insTCCGCTGCA
ENST00000667069.1:c.160_161insATGCAGCGG (MSH3)	ENSP00000499502.1:p.Ala53_Ala54insAspAlaAla
ENST00000670357.1:c.160_161insATGCAGCGG (MSH3)	ENSP00000499791.1:p.Ala53_Ala54insAspAlaAla