Canonical Allele Identifier: CA1558440947

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654962A= , CM000667.2:g.80654962A=	GRCh38
NC_000005.9:g.79950781A= , CM000667.1:g.79950781A=	GRCh37
NC_000005.8:g.79986537A=	NCBI36
NG_016607.1:g.5488A=
NG_023304.1:g.5020T=
NG_016607.2:g.5488A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-473T= (DHFR) MANE Select	NP_000782.1:n.-473T=
NM_002439.5:c.235A= (MSH3) MANE Select	NP_002430.3:p.Ile79=
ENST00000265081.7:c.235A= (MSH3) MANE Select	ENSP00000265081.6:p.Ile79=
ENST00000439211.7:c.-473T= (DHFR) MANE Select	ENSP00000396308.2:n.-473T=
NM_000791.3:c.-473T= (DHFR)	NP_000782.1:n.-473T=
NM_001290354.1:c.-579T= (DHFR)	NP_001277283.1:n.-579T=
NM_001290354.2:c.-579T= (DHFR)	NP_001277283.1:n.-579T=
NM_001290357.1:c.-473T= (DHFR)	NP_001277286.1:n.-473T=
NM_001290357.2:c.-473T= (DHFR)	NP_001277286.1:n.-473T=
NM_002439.4:c.235A= (MSH3)	NP_002430.3:p.Ile79=
NR_110936.1:n.20T= (DHFR)
NR_110936.2:n.22T= (DHFR)
ENST00000265081.6:c.235A= (MSH3)	ENSP00000265081.6:p.Ile79=
ENST00000439211.6:c.-473T= (DHFR)	ENSP00000396308.2:n.-473T=
ENST00000667069.1:c.235A= (MSH3)	ENSP00000499502.1:p.Ile79=
ENST00000670357.1:c.235A= (MSH3)	ENSP00000499791.1:p.Ile79=