Canonical Allele Identifier: CA360264829

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654758C>T , CM000667.2:g.80654758C>T	GRCh38
NC_000005.9:g.79950577C>T , CM000667.1:g.79950577C>T	GRCh37
NC_000005.8:g.79986333C>T	NCBI36
NG_016607.1:g.5284C>T
NG_023304.1:g.5224G>A
NG_016607.2:g.5284C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.31C>T (MSH3) MANE Select	ENSP00000265081.6:p.Leu11Phe
ENST00000439211.7:c.-269G>A (DHFR) MANE Select	ENSP00000396308.2:n.-269G>A
ENST00000667069.1:c.31C>T (MSH3)	ENSP00000499502.1:p.Leu11Phe
ENST00000670357.1:c.31C>T (MSH3)	ENSP00000499791.1:p.Leu11Phe
ENST00000265081.6:c.31C>T (MSH3)	ENSP00000265081.6:p.Leu11Phe
ENST00000439211.6:c.-269G>A (DHFR)	ENSP00000396308.2:n.-269G>A
NM_000791.3:c.-269G>A (DHFR)	NP_000782.1:n.-269G>A
NM_001290354.1:c.-375G>A (DHFR)	NP_001277283.1:n.-375G>A
NM_001290357.1:c.-269G>A (DHFR)	NP_001277286.1:n.-269G>A
NM_002439.4:c.31C>T (MSH3)	NP_002430.3:p.Leu11Phe
NR_110936.1:n.224G>A (DHFR)
NM_000791.4:c.-269G>A (DHFR) MANE Select	NP_000782.1:n.-269G>A
NM_002439.5:c.31C>T (MSH3) MANE Select	NP_002430.3:p.Leu11Phe
NM_001290354.2:c.-375G>A (DHFR)	NP_001277283.1:n.-375G>A
NM_001290357.2:c.-269G>A (DHFR)	NP_001277286.1:n.-269G>A
NR_110936.2:n.226G>A (DHFR)