Canonical Allele Identifier: CA915943423

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80654961_80654962delinsTG , CM000667.2:g.80654961_80654962delinsTG GRCh38
NC_000005.9:g.79950780_79950781delinsTG , CM000667.1:g.79950780_79950781delinsTG GRCh37
NC_000005.8:g.79986536_79986537delinsTG NCBI36
NG_016607.1:g.5487_5488delinsTG
NG_023304.1:g.5020_5021delinsCA
NG_016607.2:g.5487_5488delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000265081.7:c.234_235delinsTG (MSH3) MANE Select ENSP00000265081.6:p.Ile79Val
ENST00000439211.7:c.-473_-472delinsCA (DHFR) MANE Select ENSP00000396308.2:n.-473_-472delinsCA
ENST00000667069.1:c.234_235delinsTG (MSH3) ENSP00000499502.1:p.Ile79Val
ENST00000670357.1:c.234_235delinsTG (MSH3) ENSP00000499791.1:p.Ile79Val
ENST00000265081.6:c.234_235delinsTG (MSH3) ENSP00000265081.6:p.Ile79Val
ENST00000439211.6:c.-473_-472delinsCA (DHFR) ENSP00000396308.2:n.-473_-472delinsCA
NM_000791.3:c.-473_-472delinsCA (DHFR) NP_000782.1:n.-473_-472delinsCA
NM_001290354.1:c.-579_-578delinsCA (DHFR) NP_001277283.1:n.-579_-578delinsCA
NM_001290357.1:c.-473_-472delinsCA (DHFR) NP_001277286.1:n.-473_-472delinsCA
NM_002439.4:c.234_235delinsTG (MSH3) NP_002430.3:p.Ile79Val
NR_110936.1:n.20_21delinsCA (DHFR)
NM_000791.4:c.-473_-472delinsCA (DHFR) MANE Select NP_000782.1:n.-473_-472delinsCA
NM_002439.5:c.234_235delinsTG (MSH3) MANE Select NP_002430.3:p.Ile79Val
NM_001290354.2:c.-579_-578delinsCA (DHFR) NP_001277283.1:n.-579_-578delinsCA
NM_001290357.2:c.-473_-472delinsCA (DHFR) NP_001277286.1:n.-473_-472delinsCA
NR_110936.2:n.22_23delinsCA (DHFR)