Canonical Allele Identifier: CA2767179376
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80643453_80643454del , CM000667.2:g.80643453_80643454del GRCh38
NC_000005.9:g.79939272_79939273del , CM000667.1:g.79939272_79939273del GRCh37
NC_000005.8:g.79975028_79975029del NCBI36
NG_023304.1:g.16528_16529del

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.243-5445_243-5444del MANE Select ENSP00000396308.2:n.243-5445_243-5444del
ENST00000439211.6:c.243-5445_243-5444del ENSP00000396308.2:n.243-5445_243-5444del
ENST00000504396.1:c.87-5445_87-5444del ENSP00000421334.1:n.87-5445_87-5444del
ENST00000505337.5:c.243-5445_243-5444del ENSP00000426474.1:n.243-5445_243-5444del
ENST00000508282.1:n.201-5445_201-5444del
ENST00000511032.5:c.243-5445_243-5444del ENSP00000422732.1:n.243-5445_243-5444del
ENST00000513048.5:n.250+5935_250+5936del
NM_000791.3:c.243-5445_243-5444del NP_000782.1:n.243-5445_243-5444del
NM_001290354.1:c.87-5445_87-5444del NP_001277283.1:n.87-5445_87-5444del
NM_001290357.1:c.243-5445_243-5444del NP_001277286.1:n.243-5445_243-5444del
NR_110936.1:n.684+5935_684+5936del
NM_000791.4:c.243-5445_243-5444del MANE Select NP_000782.1:n.243-5445_243-5444del
NM_001290354.2:c.87-5445_87-5444del NP_001277283.1:n.87-5445_87-5444del
NM_001290357.2:c.243-5445_243-5444del NP_001277286.1:n.243-5445_243-5444del
NR_110936.2:n.686+5935_686+5936del