Canonical Allele Identifier: CA360264775

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654741A>G , CM000667.2:g.80654741A>G	GRCh38
NC_000005.9:g.79950560A>G , CM000667.1:g.79950560A>G	GRCh37
NC_000005.8:g.79986316A>G	NCBI36
NG_016607.1:g.5267A>G
NG_023304.1:g.5241T>C
NG_016607.2:g.5267A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265081.7:c.14A>G (MSH3) MANE Select	ENSP00000265081.6:p.Lys5Arg
ENST00000439211.7:c.-252T>C (DHFR) MANE Select	ENSP00000396308.2:n.-252T>C
ENST00000667069.1:c.14A>G (MSH3)	ENSP00000499502.1:p.Lys5Arg
ENST00000670357.1:c.14A>G (MSH3)	ENSP00000499791.1:p.Lys5Arg
ENST00000265081.6:c.14A>G (MSH3)	ENSP00000265081.6:p.Lys5Arg
ENST00000439211.6:c.-252T>C (DHFR)	ENSP00000396308.2:n.-252T>C
NM_000791.3:c.-252T>C (DHFR)	NP_000782.1:n.-252T>C
NM_001290354.1:c.-358T>C (DHFR)	NP_001277283.1:n.-358T>C
NM_001290357.1:c.-252T>C (DHFR)	NP_001277286.1:n.-252T>C
NM_002439.4:c.14A>G (MSH3)	NP_002430.3:p.Lys5Arg
NR_110936.1:n.241T>C (DHFR)
NM_000791.4:c.-252T>C (DHFR) MANE Select	NP_000782.1:n.-252T>C
NM_002439.5:c.14A>G (MSH3) MANE Select	NP_002430.3:p.Lys5Arg
NM_001290354.2:c.-358T>C (DHFR)	NP_001277283.1:n.-358T>C
NM_001290357.2:c.-252T>C (DHFR)	NP_001277286.1:n.-252T>C
NR_110936.2:n.243T>C (DHFR)