Canonical Allele Identifier: CA445162563
Community Standard Title: NM_000791.4(DHFR):c.231C>T (p.Ser77=)
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80649400G>A , CM000667.2:g.80649400G>A GRCh38
NC_000005.9:g.79945219G>A , CM000667.1:g.79945219G>A GRCh37
NC_000005.8:g.79980975G>A NCBI36
NG_023304.1:g.10582C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.231C>T MANE Select NP_000782.1:p.Ser77=
ENST00000439211.7:c.231C>T MANE Select ENSP00000396308.2:p.Ser77=
NM_000791.3:c.231C>T NP_000782.1:p.Ser77=
NM_001290354.1:c.75C>T NP_001277283.1:p.Ser25=
NM_001290354.2:c.75C>T NP_001277283.1:p.Ser25=
NM_001290357.1:c.231C>T NP_001277286.1:p.Ser77=
NM_001290357.2:c.231C>T NP_001277286.1:p.Ser77=
NR_110936.1:n.673C>T
NR_110936.2:n.675C>T
ENST00000439211.6:c.231C>T ENSP00000396308.2:p.Ser77=
ENST00000504396.1:c.75C>T ENSP00000421334.1:p.Ser25=
ENST00000505337.5:c.231C>T ENSP00000426474.1:p.Ser77=
ENST00000508282.1:n.189C>T
ENST00000511032.5:c.231C>T ENSP00000422732.1:p.Ser77=
ENST00000513048.5:n.239C>T
ENST00000513314.1:n.123C>T