Canonical Allele Identifier: CA1558462434
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80629003_80629006delinsTCAA , CM000667.2:g.80629003_80629006delinsTCAA GRCh38
NC_000005.9:g.79924822_79924825delinsTCAA , CM000667.1:g.79924822_79924825delinsTCAA GRCh37
NC_000005.8:g.79960578_79960581delinsTCAA NCBI36
NG_023304.1:g.30976_30979delinsTTGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*81_*84delinsTTGA MANE Select ENSP00000396308.2:n.*81_*84delinsTTGA
ENST00000439211.6:c.*81_*84delinsTTGA ENSP00000396308.2:n.*81_*84delinsTTGA
ENST00000504396.1:c.*81_*84delinsTTGA ENSP00000421334.1:n.*81_*84delinsTTGA
ENST00000505337.5:c.*48+33_*48+36delinsTTGA ENSP00000426474.1:n.*48+33_*48+36delinsTTGA
ENST00000511032.5:c.*139_*142delinsTTGA ENSP00000422732.1:n.*139_*142delinsTTGA
ENST00000513048.5:n.526_529delinsTTGA
NM_000791.3:c.*81_*84delinsTTGA NP_000782.1:n.*81_*84delinsTTGA
NM_001290354.1:c.*81_*84delinsTTGA NP_001277283.1:n.*81_*84delinsTTGA
NM_001290357.1:c.*139_*142delinsTTGA NP_001277286.1:n.*139_*142delinsTTGA
NR_110936.1:n.960_963delinsTTGA
NM_000791.4:c.*81_*84delinsTTGA MANE Select NP_000782.1:n.*81_*84delinsTTGA
NM_001290354.2:c.*81_*84delinsTTGA NP_001277283.1:n.*81_*84delinsTTGA
NM_001290357.2:c.*139_*142delinsTTGA NP_001277286.1:n.*139_*142delinsTTGA
NR_110936.2:n.962_965delinsTTGA