Canonical Allele Identifier: CA2674439539
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80633864A>G , CM000667.2:g.80633864A>G GRCh38
NC_000005.9:g.79929683A>G , CM000667.1:g.79929683A>G GRCh37
NC_000005.8:g.79965439A>G NCBI36
NG_023304.1:g.26118T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000439211.7:c.485+13T>C MANE Select ENSP00000396308.2:n.485+13T>C
ENST00000439211.6:c.485+13T>C ENSP00000396308.2:n.485+13T>C
ENST00000504396.1:c.329+13T>C ENSP00000421334.1:n.329+13T>C
ENST00000505337.5:c.485+13T>C ENSP00000426474.1:n.485+13T>C
ENST00000508282.1:n.443+13T>C
ENST00000511032.5:c.369+4019T>C ENSP00000422732.1:n.369+4019T>C
ENST00000513048.5:n.366+13T>C
NM_000791.3:c.485+13T>C NP_000782.1:n.485+13T>C
NM_001290354.1:c.329+13T>C NP_001277283.1:n.329+13T>C
NM_001290357.1:c.369+4019T>C NP_001277286.1:n.369+4019T>C
NR_110936.1:n.800+13T>C
NM_000791.4:c.485+13T>C MANE Select NP_000782.1:n.485+13T>C
NM_001290354.2:c.329+13T>C NP_001277283.1:n.329+13T>C
NM_001290357.2:c.369+4019T>C NP_001277286.1:n.369+4019T>C
NR_110936.2:n.802+13T>C