Canonical Allele Identifier: CA1558462343
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628882T= , CM000667.2:g.80628882T= GRCh38
NC_000005.9:g.79924701T= , CM000667.1:g.79924701T= GRCh37
NC_000005.8:g.79960457T= NCBI36
NG_023304.1:g.31100A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*205A= MANE Select ENSP00000396308.2:n.*205A=
ENST00000439211.6:c.*205A= ENSP00000396308.2:n.*205A=
ENST00000504396.1:c.*205A= ENSP00000421334.1:n.*205A=
ENST00000505337.5:c.*105A= ENSP00000426474.1:n.*105A=
ENST00000511032.5:c.*263A= ENSP00000422732.1:n.*263A=
ENST00000513048.5:n.650A=
NM_000791.3:c.*205A= NP_000782.1:n.*205A=
NM_001290354.1:c.*205A= NP_001277283.1:n.*205A=
NM_001290357.1:c.*263A= NP_001277286.1:n.*263A=
NR_110936.1:n.1084A=
NM_000791.4:c.*205A= MANE Select NP_000782.1:n.*205A=
NM_001290354.2:c.*205A= NP_001277283.1:n.*205A=
NM_001290357.2:c.*263A= NP_001277286.1:n.*263A=
NR_110936.2:n.1086A=