Canonical Allele Identifier: CA2674440961
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80654344_80654345insTGGCGCATCCCGCCCAGGT , CM000667.2:g.80654344_80654345insTGGCGCATCCCGCCCAGGT GRCh38
NC_000005.9:g.79950163_79950164insTGGCGCATCCCGCCCAGGT , CM000667.1:g.79950163_79950164insTGGCGCATCCCGCCCAGGT GRCh37
NC_000005.8:g.79985919_79985920insTGGCGCATCCCGCCCAGGT NCBI36
NG_016607.1:g.4870_4871insTGGCGCATCCCGCCCAGGT
NG_023304.1:g.5637_5638insACCTGGGCGGGATGCGCCA
NG_016607.2:g.4870_4871insTGGCGCATCCCGCCCAGGT

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.86+59_86+60insACCTGGGCGGGATGCGCCA MANE Select NP_000782.1:n.86+59_86+60insACCTGGGCGGGATGCGCCA
ENST00000439211.7:c.86+59_86+60insACCTGGGCGGGATGCGCCA MANE Select ENSP00000396308.2:n.86+59_86+60insACCTGGGCGGGATGCGCCA
NM_000791.3:c.86+59_86+60insACCTGGGCGGGATGCGCCA NP_000782.1:n.86+59_86+60insACCTGGGCGGGATGCGCCA
NM_001290354.1:c.-21+59_-21+60insACCTGGGCGGGATGCGCCA NP_001277283.1:n.-21+59_-21+60insACCTGGGCGGGATGCGCCA
NM_001290354.2:c.-21+59_-21+60insACCTGGGCGGGATGCGCCA NP_001277283.1:n.-21+59_-21+60insACCTGGGCGGGATGCGCCA
NM_001290357.1:c.86+59_86+60insACCTGGGCGGGATGCGCCA NP_001277286.1:n.86+59_86+60insACCTGGGCGGGATGCGCCA
NM_001290357.2:c.86+59_86+60insACCTGGGCGGGATGCGCCA NP_001277286.1:n.86+59_86+60insACCTGGGCGGGATGCGCCA
NR_110936.1:n.578+59_578+60insACCTGGGCGGGATGCGCCA
NR_110936.2:n.580+59_580+60insACCTGGGCGGGATGCGCCA
ENST00000439211.6:c.86+59_86+60insACCTGGGCGGGATGCGCCA ENSP00000396308.2:n.86+59_86+60insACCTGGGCGGGATGCGCCA
ENST00000504396.1:c.-21+59_-21+60insACCTGGGCGGGATGCGCCA ENSP00000421334.1:n.-21+59_-21+60insACCTGGGCGGGATGCGCCA
ENST00000505337.5:c.86+59_86+60insACCTGGGCGGGATGCGCCA ENSP00000426474.1:n.86+59_86+60insACCTGGGCGGGATGCGCCA
ENST00000511032.5:c.86+59_86+60insACCTGGGCGGGATGCGCCA ENSP00000422732.1:n.86+59_86+60insACCTGGGCGGGATGCGCCA
ENST00000513048.5:n.144+59_144+60insACCTGGGCGGGATGCGCCA