Canonical Allele Identifier: CA2767179380
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80643461C>T , CM000667.2:g.80643461C>T GRCh38
NC_000005.9:g.79939280C>T , CM000667.1:g.79939280C>T GRCh37
NC_000005.8:g.79975036C>T NCBI36
NG_023304.1:g.16521G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.243-5452G>A MANE Select ENSP00000396308.2:n.243-5452G>A
ENST00000439211.6:c.243-5452G>A ENSP00000396308.2:n.243-5452G>A
ENST00000504396.1:c.87-5452G>A ENSP00000421334.1:n.87-5452G>A
ENST00000505337.5:c.243-5452G>A ENSP00000426474.1:n.243-5452G>A
ENST00000508282.1:n.201-5452G>A
ENST00000511032.5:c.243-5452G>A ENSP00000422732.1:n.243-5452G>A
ENST00000513048.5:n.250+5928G>A
NM_000791.3:c.243-5452G>A NP_000782.1:n.243-5452G>A
NM_001290354.1:c.87-5452G>A NP_001277283.1:n.87-5452G>A
NM_001290357.1:c.243-5452G>A NP_001277286.1:n.243-5452G>A
NR_110936.1:n.684+5928G>A
NM_000791.4:c.243-5452G>A MANE Select NP_000782.1:n.243-5452G>A
NM_001290354.2:c.87-5452G>A NP_001277283.1:n.87-5452G>A
NM_001290357.2:c.243-5452G>A NP_001277286.1:n.243-5452G>A
NR_110936.2:n.686+5928G>A