Canonical Allele Identifier: CA2767178944
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80628878_80628879insTCATTAAAAAA , CM000667.2:g.80628878_80628879insTCATTAAAAAA GRCh38
NC_000005.9:g.79924697_79924698insTCATTAAAAAA , CM000667.1:g.79924697_79924698insTCATTAAAAAA GRCh37
NC_000005.8:g.79960453_79960454insTCATTAAAAAA NCBI36
NG_023304.1:g.31103_31104insTTTTTTAATGA

Transcript Alleles

HGVS Amino-acid change
ENST00000439211.7:c.*208_*209insTTTTTTAATGA MANE Select ENSP00000396308.2:n.*208_*209insTTTTTTAATGA
ENST00000439211.6:c.*208_*209insTTTTTTAATGA ENSP00000396308.2:n.*208_*209insTTTTTTAATGA
ENST00000504396.1:c.*208_*209insTTTTTTAATGA ENSP00000421334.1:n.*208_*209insTTTTTTAATGA
ENST00000505337.5:c.*108_*109insTTTTTTAATGA ENSP00000426474.1:n.*108_*109insTTTTTTAATGA
ENST00000511032.5:c.*266_*267insTTTTTTAATGA ENSP00000422732.1:n.*266_*267insTTTTTTAATGA
ENST00000513048.5:n.653_654insTTTTTTAATGA
NM_000791.3:c.*208_*209insTTTTTTAATGA NP_000782.1:n.*208_*209insTTTTTTAATGA
NM_001290354.1:c.*208_*209insTTTTTTAATGA NP_001277283.1:n.*208_*209insTTTTTTAATGA
NM_001290357.1:c.*266_*267insTTTTTTAATGA NP_001277286.1:n.*266_*267insTTTTTTAATGA
NR_110936.1:n.1087_1088insTTTTTTAATGA
NM_000791.4:c.*208_*209insTTTTTTAATGA MANE Select NP_000782.1:n.*208_*209insTTTTTTAATGA
NM_001290354.2:c.*208_*209insTTTTTTAATGA NP_001277283.1:n.*208_*209insTTTTTTAATGA
NM_001290357.2:c.*266_*267insTTTTTTAATGA NP_001277286.1:n.*266_*267insTTTTTTAATGA
NR_110936.2:n.1089_1090insTTTTTTAATGA