Canonical Allele Identifier: CA1558462423
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628989_80628991delinsTTA , CM000667.2:g.80628989_80628991delinsTTA GRCh38
NC_000005.9:g.79924808_79924810delinsTTA , CM000667.1:g.79924808_79924810delinsTTA GRCh37
NC_000005.8:g.79960564_79960566delinsTTA NCBI36
NG_023304.1:g.30991_30993delinsTAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*96_*98delinsTAA MANE Select ENSP00000396308.2:n.*96_*98delinsTAA
ENST00000439211.6:c.*96_*98delinsTAA ENSP00000396308.2:n.*96_*98delinsTAA
ENST00000504396.1:c.*96_*98delinsTAA ENSP00000421334.1:n.*96_*98delinsTAA
ENST00000505337.5:c.*48+48_*49-51delinsTAA ENSP00000426474.1:n.*48+48_*49-51delinsTAA
ENST00000511032.5:c.*154_*156delinsTAA ENSP00000422732.1:n.*154_*156delinsTAA
ENST00000513048.5:n.541_543delinsTAA
NM_000791.3:c.*96_*98delinsTAA NP_000782.1:n.*96_*98delinsTAA
NM_001290354.1:c.*96_*98delinsTAA NP_001277283.1:n.*96_*98delinsTAA
NM_001290357.1:c.*154_*156delinsTAA NP_001277286.1:n.*154_*156delinsTAA
NR_110936.1:n.975_977delinsTAA
NM_000791.4:c.*96_*98delinsTAA MANE Select NP_000782.1:n.*96_*98delinsTAA
NM_001290354.2:c.*96_*98delinsTAA NP_001277283.1:n.*96_*98delinsTAA
NM_001290357.2:c.*154_*156delinsTAA NP_001277286.1:n.*154_*156delinsTAA
NR_110936.2:n.977_979delinsTAA