Canonical Allele Identifier: CA3327426

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654783C>G , CM000667.2:g.80654783C>G	GRCh38
NC_000005.9:g.79950602C>G , CM000667.1:g.79950602C>G	GRCh37
NC_000005.8:g.79986358C>G	NCBI36
NG_016607.1:g.5309C>G
NG_023304.1:g.5199G>C
NG_016607.2:g.5309C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.56C>G (MSH3) MANE Select	ENSP00000265081.6:p.Ala19Gly
ENST00000439211.7:c.-294G>C (DHFR) MANE Select	ENSP00000396308.2:n.-294G>C
ENST00000667069.1:c.56C>G (MSH3)	ENSP00000499502.1:p.Ala19Gly
ENST00000670357.1:c.56C>G (MSH3)	ENSP00000499791.1:p.Ala19Gly
ENST00000265081.6:c.56C>G (MSH3)	ENSP00000265081.6:p.Ala19Gly
ENST00000439211.6:c.-294G>C (DHFR)	ENSP00000396308.2:n.-294G>C
NM_000791.3:c.-294G>C (DHFR)	NP_000782.1:n.-294G>C
NM_001290354.1:c.-400G>C (DHFR)	NP_001277283.1:n.-400G>C
NM_001290357.1:c.-294G>C (DHFR)	NP_001277286.1:n.-294G>C
NM_002439.4:c.56C>G (MSH3)	NP_002430.3:p.Ala19Gly
NR_110936.1:n.199G>C (DHFR)
NM_000791.4:c.-294G>C (DHFR) MANE Select	NP_000782.1:n.-294G>C
NM_002439.5:c.56C>G (MSH3) MANE Select	NP_002430.3:p.Ala19Gly
NM_001290354.2:c.-400G>C (DHFR)	NP_001277283.1:n.-400G>C
NM_001290357.2:c.-294G>C (DHFR)	NP_001277286.1:n.-294G>C
NR_110936.2:n.201G>C (DHFR)