Canonical Allele Identifier: CA360261542
Community Standard Title: NM_000791.4(DHFR):c.194A>G (p.Asn65Ser)
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80649437T>C , CM000667.2:g.80649437T>C GRCh38
NC_000005.9:g.79945256T>C , CM000667.1:g.79945256T>C GRCh37
NC_000005.8:g.79981012T>C NCBI36
NG_023304.1:g.10545A>G

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.194A>G MANE Select NP_000782.1:p.Asn65Ser
ENST00000439211.7:c.194A>G MANE Select ENSP00000396308.2:p.Asn65Ser
NM_000791.3:c.194A>G NP_000782.1:p.Asn65Ser
NM_001290354.1:c.38A>G NP_001277283.1:p.Asn13Ser
NM_001290354.2:c.38A>G NP_001277283.1:p.Asn13Ser
NM_001290357.1:c.194A>G NP_001277286.1:p.Asn65Ser
NM_001290357.2:c.194A>G NP_001277286.1:p.Asn65Ser
NR_110936.1:n.636A>G
NR_110936.2:n.638A>G
ENST00000439211.6:c.194A>G ENSP00000396308.2:p.Asn65Ser
ENST00000504396.1:c.38A>G ENSP00000421334.1:p.Asn13Ser
ENST00000505337.5:c.194A>G ENSP00000426474.1:p.Asn65Ser
ENST00000508282.1:n.152A>G
ENST00000511032.5:c.194A>G ENSP00000422732.1:p.Asn65Ser
ENST00000513048.5:n.202A>G
ENST00000513314.1:n.86A>G