Canonical Allele Identifier: CA3327176
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80633922G>A , CM000667.2:g.80633922G>A GRCh38
NC_000005.9:g.79929741G>A , CM000667.1:g.79929741G>A GRCh37
NC_000005.8:g.79965497G>A NCBI36
NG_023304.1:g.26060C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.440C>T MANE Select ENSP00000396308.2:p.Thr147Met
ENST00000439211.6:c.440C>T ENSP00000396308.2:p.Thr147Met
ENST00000504396.1:c.284C>T ENSP00000421334.1:p.Thr95Met
ENST00000505337.5:c.440C>T ENSP00000426474.1:p.Thr147Met
ENST00000508282.1:n.398C>T
ENST00000511032.5:c.369+3961C>T ENSP00000422732.1:n.369+3961C>T
ENST00000513048.5:n.321C>T
NM_000791.3:c.440C>T NP_000782.1:p.Thr147Met
NM_001290354.1:c.284C>T NP_001277283.1:p.Thr95Met
NM_001290357.1:c.369+3961C>T NP_001277286.1:n.369+3961C>T
NR_110936.1:n.755C>T
NM_000791.4:c.440C>T MANE Select NP_000782.1:p.Thr147Met
NM_001290354.2:c.284C>T NP_001277283.1:p.Thr95Met
NM_001290357.2:c.369+3961C>T NP_001277286.1:n.369+3961C>T
NR_110936.2:n.757C>T