Canonical Allele Identifier: CA3327208
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80637958T>C , CM000667.2:g.80637958T>C GRCh38
NC_000005.9:g.79933777T>C , CM000667.1:g.79933777T>C GRCh37
NC_000005.8:g.79969533T>C NCBI36
NG_023304.1:g.22024A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.294A>G MANE Select ENSP00000396308.2:p.Leu98=
ENST00000439211.6:c.294A>G ENSP00000396308.2:p.Leu98=
ENST00000504396.1:c.138A>G ENSP00000421334.1:p.Leu46=
ENST00000505337.5:c.294A>G ENSP00000426474.1:p.Leu98=
ENST00000508282.1:n.252A>G
ENST00000511032.5:c.294A>G ENSP00000422732.1:p.Leu98=
ENST00000513048.5:n.251-3966A>G
NM_000791.3:c.294A>G NP_000782.1:p.Leu98=
NM_001290354.1:c.138A>G NP_001277283.1:p.Leu46=
NM_001290357.1:c.294A>G NP_001277286.1:p.Leu98=
NR_110936.1:n.685-3966A>G
NM_000791.4:c.294A>G MANE Select NP_000782.1:p.Leu98=
NM_001290354.2:c.138A>G NP_001277283.1:p.Leu46=
NM_001290357.2:c.294A>G NP_001277286.1:p.Leu98=
NR_110936.2:n.687-3966A>G