Canonical Allele Identifier: CA1558462359
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628892T= , CM000667.2:g.80628892T= GRCh38
NC_000005.9:g.79924711T= , CM000667.1:g.79924711T= GRCh37
NC_000005.8:g.79960467T= NCBI36
NG_023304.1:g.31090A=

Transcript Alleles

HGVS Amino-acid change
ENST00000439211.7:c.*195A= MANE Select ENSP00000396308.2:n.*195A=
ENST00000439211.6:c.*195A= ENSP00000396308.2:n.*195A=
ENST00000504396.1:c.*195A= ENSP00000421334.1:n.*195A=
ENST00000505337.5:c.*95A= ENSP00000426474.1:n.*95A=
ENST00000511032.5:c.*253A= ENSP00000422732.1:n.*253A=
ENST00000513048.5:n.640A=
NM_000791.3:c.*195A= NP_000782.1:n.*195A=
NM_001290354.1:c.*195A= NP_001277283.1:n.*195A=
NM_001290357.1:c.*253A= NP_001277286.1:n.*253A=
NR_110936.1:n.1074A=
NM_000791.4:c.*195A= MANE Select NP_000782.1:n.*195A=
NM_001290354.2:c.*195A= NP_001277283.1:n.*195A=
NM_001290357.2:c.*253A= NP_001277286.1:n.*253A=
NR_110936.2:n.1076A=