Canonical Allele Identifier: CA445393933

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654886G>A , CM000667.2:g.80654886G>A	GRCh38
NC_000005.9:g.79950705G>A , CM000667.1:g.79950705G>A	GRCh37
NC_000005.8:g.79986461G>A	NCBI36
NG_016607.1:g.5412G>A
NG_023304.1:g.5096C>T
NG_016607.2:g.5412G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-397C>T (DHFR) MANE Select	NP_000782.1:n.-397C>T
NM_002439.5:c.159G>A (MSH3) MANE Select	NP_002430.3:p.Ala53=
ENST00000265081.7:c.159G>A (MSH3) MANE Select	ENSP00000265081.6:p.Ala53=
ENST00000439211.7:c.-397C>T (DHFR) MANE Select	ENSP00000396308.2:n.-397C>T
NM_000791.3:c.-397C>T (DHFR)	NP_000782.1:n.-397C>T
NM_001290354.1:c.-503C>T (DHFR)	NP_001277283.1:n.-503C>T
NM_001290354.2:c.-503C>T (DHFR)	NP_001277283.1:n.-503C>T
NM_001290357.1:c.-397C>T (DHFR)	NP_001277286.1:n.-397C>T
NM_001290357.2:c.-397C>T (DHFR)	NP_001277286.1:n.-397C>T
NM_002439.4:c.159G>A (MSH3)	NP_002430.3:p.Ala53=
NR_110936.1:n.96C>T (DHFR)
NR_110936.2:n.98C>T (DHFR)
ENST00000265081.6:c.159G>A (MSH3)	ENSP00000265081.6:p.Ala53=
ENST00000439211.6:c.-397C>T (DHFR)	ENSP00000396308.2:n.-397C>T
ENST00000667069.1:c.159G>A (MSH3)	ENSP00000499502.1:p.Ala53=
ENST00000670357.1:c.159G>A (MSH3)	ENSP00000499791.1:p.Ala53=