Canonical Allele Identifier: CA1558472377
Community Standard Title: NM_000791.4(DHFR):c.243-1008A=
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80639017T= , CM000667.2:g.80639017T= GRCh38
NC_000005.9:g.79934836T= , CM000667.1:g.79934836T= GRCh37
NC_000005.8:g.79970592T= NCBI36
NG_023304.1:g.20965A=

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.243-1008A= MANE Select NP_000782.1:n.243-1008A=
ENST00000439211.7:c.243-1008A= MANE Select ENSP00000396308.2:n.243-1008A=
NM_000791.3:c.243-1008A= NP_000782.1:n.243-1008A=
NM_001290354.1:c.87-1008A= NP_001277283.1:n.87-1008A=
NM_001290354.2:c.87-1008A= NP_001277283.1:n.87-1008A=
NM_001290357.1:c.243-1008A= NP_001277286.1:n.243-1008A=
NM_001290357.2:c.243-1008A= NP_001277286.1:n.243-1008A=
NR_110936.1:n.685-5025A=
NR_110936.2:n.687-5025A=
ENST00000439211.6:c.243-1008A= ENSP00000396308.2:n.243-1008A=
ENST00000504396.1:c.87-1008A= ENSP00000421334.1:n.87-1008A=
ENST00000505337.5:c.243-1008A= ENSP00000426474.1:n.243-1008A=
ENST00000508282.1:n.201-1008A=
ENST00000511032.5:c.243-1008A= ENSP00000422732.1:n.243-1008A=
ENST00000513048.5:n.251-5025A=