Canonical Allele Identifier: CA3327184
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80634008_80634010del , CM000667.2:g.80634008_80634010del GRCh38
NC_000005.9:g.79929827_79929829del , CM000667.1:g.79929827_79929829del GRCh37
NC_000005.8:g.79965583_79965585del NCBI36
NG_023304.1:g.25976_25978del

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.370-14_370-12del MANE Select NP_000782.1:n.370-14_370-12del
ENST00000439211.7:c.370-14_370-12del MANE Select ENSP00000396308.2:n.370-14_370-12del
NM_000791.3:c.370-14_370-12del NP_000782.1:n.370-14_370-12del
NM_001290354.1:c.214-14_214-12del NP_001277283.1:n.214-14_214-12del
NM_001290354.2:c.214-14_214-12del NP_001277283.1:n.214-14_214-12del
NM_001290357.1:c.369+3877_369+3879del NP_001277286.1:n.369+3877_369+3879del
NM_001290357.2:c.369+3877_369+3879del NP_001277286.1:n.369+3877_369+3879del
NR_110936.1:n.685-14_685-12del
NR_110936.2:n.687-14_687-12del
ENST00000439211.6:c.370-14_370-12del ENSP00000396308.2:n.370-14_370-12del
ENST00000504396.1:c.214-14_214-12del ENSP00000421334.1:n.214-14_214-12del
ENST00000505337.5:c.370-14_370-12del ENSP00000426474.1:n.370-14_370-12del
ENST00000508282.1:n.328-14_328-12del
ENST00000511032.5:c.369+3877_369+3879del ENSP00000422732.1:n.369+3877_369+3879del
ENST00000513048.5:n.251-14_251-12del