Canonical Allele Identifier: CA3327429

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80654804G>A , CM000667.2:g.80654804G>A GRCh38
NC_000005.9:g.79950623G>A , CM000667.1:g.79950623G>A GRCh37
NC_000005.8:g.79986379G>A NCBI36
NG_016607.1:g.5330G>A
NG_023304.1:g.5178C>T
NG_016607.2:g.5330G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.77G>A (MSH3) MANE Select ENSP00000265081.6:p.Arg26Gln
ENST00000439211.7:c.-315C>T (DHFR) MANE Select ENSP00000396308.2:n.-315C>T
ENST00000667069.1:c.77G>A (MSH3) ENSP00000499502.1:p.Arg26Gln
ENST00000670357.1:c.77G>A (MSH3) ENSP00000499791.1:p.Arg26Gln
ENST00000265081.6:c.77G>A (MSH3) ENSP00000265081.6:p.Arg26Gln
ENST00000439211.6:c.-315C>T (DHFR) ENSP00000396308.2:n.-315C>T
NM_000791.3:c.-315C>T (DHFR) NP_000782.1:n.-315C>T
NM_001290354.1:c.-421C>T (DHFR) NP_001277283.1:n.-421C>T
NM_001290357.1:c.-315C>T (DHFR) NP_001277286.1:n.-315C>T
NM_002439.4:c.77G>A (MSH3) NP_002430.3:p.Arg26Gln
NR_110936.1:n.178C>T (DHFR)
NM_000791.4:c.-315C>T (DHFR) MANE Select NP_000782.1:n.-315C>T
NM_002439.5:c.77G>A (MSH3) MANE Select NP_002430.3:p.Arg26Gln
NM_001290354.2:c.-421C>T (DHFR) NP_001277283.1:n.-421C>T
NM_001290357.2:c.-315C>T (DHFR) NP_001277286.1:n.-315C>T
NR_110936.2:n.180C>T (DHFR)