Canonical Allele Identifier: CA1558436668
Community Standard Title: NM_000791.4(DHFR):c.238C= (p.Leu80=)
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80649393G= , CM000667.2:g.80649393G= GRCh38
NC_000005.9:g.79945212G= , CM000667.1:g.79945212G= GRCh37
NC_000005.8:g.79980968G= NCBI36
NG_023304.1:g.10589C=

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.238C= MANE Select NP_000782.1:p.Leu80=
ENST00000439211.7:c.238C= MANE Select ENSP00000396308.2:p.Leu80=
NM_000791.3:c.238C= NP_000782.1:p.Leu80=
NM_001290354.1:c.82C= NP_001277283.1:p.Leu28=
NM_001290354.2:c.82C= NP_001277283.1:p.Leu28=
NM_001290357.1:c.238C= NP_001277286.1:p.Leu80=
NM_001290357.2:c.238C= NP_001277286.1:p.Leu80=
NR_110936.1:n.680C=
NR_110936.2:n.682C=
ENST00000439211.6:c.238C= ENSP00000396308.2:p.Leu80=
ENST00000504396.1:c.82C= ENSP00000421334.1:p.Leu28=
ENST00000505337.5:c.238C= ENSP00000426474.1:p.Leu80=
ENST00000508282.1:n.196C=
ENST00000511032.5:c.238C= ENSP00000422732.1:p.Leu80=
ENST00000513048.5:n.246C=
ENST00000513314.1:n.130C=