Canonical Allele Identifier: CA1558476277
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80643496G= , CM000667.2:g.80643496G= GRCh38
NC_000005.9:g.79939315G= , CM000667.1:g.79939315G= GRCh37
NC_000005.8:g.79975071G= NCBI36
NG_023304.1:g.16486C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.243-5487C= MANE Select ENSP00000396308.2:n.243-5487C=
ENST00000439211.6:c.243-5487C= ENSP00000396308.2:n.243-5487C=
ENST00000504396.1:c.87-5487C= ENSP00000421334.1:n.87-5487C=
ENST00000505337.5:c.243-5487C= ENSP00000426474.1:n.243-5487C=
ENST00000508282.1:n.201-5487C=
ENST00000511032.5:c.243-5487C= ENSP00000422732.1:n.243-5487C=
ENST00000513048.5:n.250+5893C=
NM_000791.3:c.243-5487C= NP_000782.1:n.243-5487C=
NM_001290354.1:c.87-5487C= NP_001277283.1:n.87-5487C=
NM_001290357.1:c.243-5487C= NP_001277286.1:n.243-5487C=
NR_110936.1:n.684+5893C=
NM_000791.4:c.243-5487C= MANE Select NP_000782.1:n.243-5487C=
NM_001290354.2:c.87-5487C= NP_001277283.1:n.87-5487C=
NM_001290357.2:c.243-5487C= NP_001277286.1:n.243-5487C=
NR_110936.2:n.686+5893C=