Canonical Allele Identifier: CA360265754

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654966T>C , CM000667.2:g.80654966T>C	GRCh38
NC_000005.9:g.79950785T>C , CM000667.1:g.79950785T>C	GRCh37
NC_000005.8:g.79986541T>C	NCBI36
NG_016607.1:g.5492T>C
NG_023304.1:g.5016A>G
NG_016607.2:g.5492T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-477A>G (DHFR) MANE Select	NP_000782.1:n.-477A>G
NM_002439.5:c.237+2T>C (MSH3) MANE Select	NP_002430.3:n.237+2T>C
ENST00000265081.7:c.237+2T>C (MSH3) MANE Select	ENSP00000265081.6:n.237+2T>C
ENST00000439211.7:c.-477A>G (DHFR) MANE Select	ENSP00000396308.2:n.-477A>G
NM_000791.3:c.-477A>G (DHFR)	NP_000782.1:n.-477A>G
NM_001290354.1:c.-583A>G (DHFR)	NP_001277283.1:n.-583A>G
NM_001290354.2:c.-583A>G (DHFR)	NP_001277283.1:n.-583A>G
NM_001290357.1:c.-477A>G (DHFR)	NP_001277286.1:n.-477A>G
NM_001290357.2:c.-477A>G (DHFR)	NP_001277286.1:n.-477A>G
NM_002439.4:c.237+2T>C (MSH3)	NP_002430.3:n.237+2T>C
NR_110936.1:n.16A>G (DHFR)
NR_110936.2:n.18A>G (DHFR)
ENST00000265081.6:c.237+2T>C (MSH3)	ENSP00000265081.6:n.237+2T>C
ENST00000439211.6:c.-477A>G (DHFR)	ENSP00000396308.2:n.-477A>G
ENST00000667069.1:c.237+2T>C (MSH3)	ENSP00000499502.1:n.237+2T>C
ENST00000670357.1:c.237+2T>C (MSH3)	ENSP00000499791.1:n.237+2T>C