Canonical Allele Identifier: CA360265252

Gene: MSH3 DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80654812C>T , CM000667.2:g.80654812C>T	GRCh38
NC_000005.9:g.79950631C>T , CM000667.1:g.79950631C>T	GRCh37
NC_000005.8:g.79986387C>T	NCBI36
NG_016607.1:g.5338C>T
NG_023304.1:g.5170G>A
NG_016607.2:g.5338C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.-323G>A (DHFR) MANE Select	NP_000782.1:n.-323G>A
NM_002439.5:c.85C>T (MSH3) MANE Select	NP_002430.3:p.Gln29Ter
ENST00000265081.7:c.85C>T (MSH3) MANE Select	ENSP00000265081.6:p.Gln29Ter
ENST00000439211.7:c.-323G>A (DHFR) MANE Select	ENSP00000396308.2:n.-323G>A
NM_000791.3:c.-323G>A (DHFR)	NP_000782.1:n.-323G>A
NM_001290354.1:c.-429G>A (DHFR)	NP_001277283.1:n.-429G>A
NM_001290354.2:c.-429G>A (DHFR)	NP_001277283.1:n.-429G>A
NM_001290357.1:c.-323G>A (DHFR)	NP_001277286.1:n.-323G>A
NM_001290357.2:c.-323G>A (DHFR)	NP_001277286.1:n.-323G>A
NM_002439.4:c.85C>T (MSH3)	NP_002430.3:p.Gln29Ter
NR_110936.1:n.170G>A (DHFR)
NR_110936.2:n.172G>A (DHFR)
ENST00000265081.6:c.85C>T (MSH3)	ENSP00000265081.6:p.Gln29Ter
ENST00000439211.6:c.-323G>A (DHFR)	ENSP00000396308.2:n.-323G>A
ENST00000667069.1:c.85C>T (MSH3)	ENSP00000499502.1:p.Gln29Ter
ENST00000670357.1:c.85C>T (MSH3)	ENSP00000499791.1:p.Gln29Ter