Canonical Allele Identifier: CA360257125
Community Standard Title: NM_000791.4(DHFR):c.392A>G (p.His131Arg)
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80633970T>C , CM000667.2:g.80633970T>C GRCh38
NC_000005.9:g.79929789T>C , CM000667.1:g.79929789T>C GRCh37
NC_000005.8:g.79965545T>C NCBI36
NG_023304.1:g.26012A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.392A>G MANE Select NP_000782.1:p.His131Arg
ENST00000439211.7:c.392A>G MANE Select ENSP00000396308.2:p.His131Arg
NM_000791.3:c.392A>G NP_000782.1:p.His131Arg
NM_001290354.1:c.236A>G NP_001277283.1:p.His79Arg
NM_001290354.2:c.236A>G NP_001277283.1:p.His79Arg
NM_001290357.1:c.369+3913A>G NP_001277286.1:n.369+3913A>G
NM_001290357.2:c.369+3913A>G NP_001277286.1:n.369+3913A>G
NR_110936.1:n.707A>G
NR_110936.2:n.709A>G
ENST00000439211.6:c.392A>G ENSP00000396308.2:p.His131Arg
ENST00000504396.1:c.236A>G ENSP00000421334.1:p.His79Arg
ENST00000505337.5:c.392A>G ENSP00000426474.1:p.His131Arg
ENST00000508282.1:n.350A>G
ENST00000511032.5:c.369+3913A>G ENSP00000422732.1:n.369+3913A>G
ENST00000513048.5:n.273A>G