Canonical Allele Identifier: CA2565474406
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628979_80628980del , CM000667.2:g.80628979_80628980del GRCh38
NC_000005.9:g.79924798_79924799del , CM000667.1:g.79924798_79924799del GRCh37
NC_000005.8:g.79960554_79960555del NCBI36
NG_023304.1:g.31002_31003del

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.*107_*108del MANE Select ENSP00000396308.2:n.*107_*108del
ENST00000439211.6:c.*107_*108del ENSP00000396308.2:n.*107_*108del
ENST00000504396.1:c.*107_*108del ENSP00000421334.1:n.*107_*108del
ENST00000505337.5:c.*49-42_*49-41del ENSP00000426474.1:n.*49-42_*49-41del
ENST00000511032.5:c.*165_*166del ENSP00000422732.1:n.*165_*166del
ENST00000513048.5:n.552_553del
NM_000791.3:c.*107_*108del NP_000782.1:n.*107_*108del
NM_001290354.1:c.*107_*108del NP_001277283.1:n.*107_*108del
NM_001290357.1:c.*165_*166del NP_001277286.1:n.*165_*166del
NR_110936.1:n.986_987del
NM_000791.4:c.*107_*108del MANE Select NP_000782.1:n.*107_*108del
NM_001290354.2:c.*107_*108del NP_001277283.1:n.*107_*108del
NM_001290357.2:c.*165_*166del NP_001277286.1:n.*165_*166del
NR_110936.2:n.988_989del