Canonical Allele Identifier: CA1558476191
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80643443T= , CM000667.2:g.80643443T= GRCh38
NC_000005.9:g.79939262T= , CM000667.1:g.79939262T= GRCh37
NC_000005.8:g.79975018T= NCBI36
NG_023304.1:g.16539A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.243-5434A= MANE Select ENSP00000396308.2:n.243-5434A=
ENST00000439211.6:c.243-5434A= ENSP00000396308.2:n.243-5434A=
ENST00000504396.1:c.87-5434A= ENSP00000421334.1:n.87-5434A=
ENST00000505337.5:c.243-5434A= ENSP00000426474.1:n.243-5434A=
ENST00000508282.1:n.201-5434A=
ENST00000511032.5:c.243-5434A= ENSP00000422732.1:n.243-5434A=
ENST00000513048.5:n.250+5946A=
NM_000791.3:c.243-5434A= NP_000782.1:n.243-5434A=
NM_001290354.1:c.87-5434A= NP_001277283.1:n.87-5434A=
NM_001290357.1:c.243-5434A= NP_001277286.1:n.243-5434A=
NR_110936.1:n.684+5946A=
NM_000791.4:c.243-5434A= MANE Select NP_000782.1:n.243-5434A=
NM_001290354.2:c.87-5434A= NP_001277283.1:n.87-5434A=
NM_001290357.2:c.243-5434A= NP_001277286.1:n.243-5434A=
NR_110936.2:n.686+5946A=