Canonical Allele Identifier: CA1558462354
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628887T= , CM000667.2:g.80628887T= GRCh38
NC_000005.9:g.79924706T= , CM000667.1:g.79924706T= GRCh37
NC_000005.8:g.79960462T= NCBI36
NG_023304.1:g.31095A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*200A= MANE Select ENSP00000396308.2:n.*200A=
ENST00000439211.6:c.*200A= ENSP00000396308.2:n.*200A=
ENST00000504396.1:c.*200A= ENSP00000421334.1:n.*200A=
ENST00000505337.5:c.*100A= ENSP00000426474.1:n.*100A=
ENST00000511032.5:c.*258A= ENSP00000422732.1:n.*258A=
ENST00000513048.5:n.645A=
NM_000791.3:c.*200A= NP_000782.1:n.*200A=
NM_001290354.1:c.*200A= NP_001277283.1:n.*200A=
NM_001290357.1:c.*258A= NP_001277286.1:n.*258A=
NR_110936.1:n.1079A=
NM_000791.4:c.*200A= MANE Select NP_000782.1:n.*200A=
NM_001290354.2:c.*200A= NP_001277283.1:n.*200A=
NM_001290357.2:c.*258A= NP_001277286.1:n.*258A=
NR_110936.2:n.1081A=