Canonical Allele Identifier: CA2767179382
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80643470_80643471insC , CM000667.2:g.80643470_80643471insC GRCh38
NC_000005.9:g.79939289_79939290insC , CM000667.1:g.79939289_79939290insC GRCh37
NC_000005.8:g.79975045_79975046insC NCBI36
NG_023304.1:g.16511_16512insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.243-5462_243-5461insG MANE Select ENSP00000396308.2:n.243-5462_243-5461insG
ENST00000439211.6:c.243-5462_243-5461insG ENSP00000396308.2:n.243-5462_243-5461insG
ENST00000504396.1:c.87-5462_87-5461insG ENSP00000421334.1:n.87-5462_87-5461insG
ENST00000505337.5:c.243-5462_243-5461insG ENSP00000426474.1:n.243-5462_243-5461insG
ENST00000508282.1:n.201-5462_201-5461insG
ENST00000511032.5:c.243-5462_243-5461insG ENSP00000422732.1:n.243-5462_243-5461insG
ENST00000513048.5:n.250+5918_250+5919insG
NM_000791.3:c.243-5462_243-5461insG NP_000782.1:n.243-5462_243-5461insG
NM_001290354.1:c.87-5462_87-5461insG NP_001277283.1:n.87-5462_87-5461insG
NM_001290357.1:c.243-5462_243-5461insG NP_001277286.1:n.243-5462_243-5461insG
NR_110936.1:n.684+5918_684+5919insG
NM_000791.4:c.243-5462_243-5461insG MANE Select NP_000782.1:n.243-5462_243-5461insG
NM_001290354.2:c.87-5462_87-5461insG NP_001277283.1:n.87-5462_87-5461insG
NM_001290357.2:c.243-5462_243-5461insG NP_001277286.1:n.243-5462_243-5461insG
NR_110936.2:n.686+5918_686+5919insG