Canonical Allele Identifier: CA1558467039
Community Standard Title: NM_000791.4(DHFR):c.458A= (p.Asp153=)
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80633904T= , CM000667.2:g.80633904T= GRCh38
NC_000005.9:g.79929723T= , CM000667.1:g.79929723T= GRCh37
NC_000005.8:g.79965479T= NCBI36
NG_023304.1:g.26078A=

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.458A= MANE Select NP_000782.1:p.Asp153=
ENST00000439211.7:c.458A= MANE Select ENSP00000396308.2:p.Asp153=
NM_000791.3:c.458A= NP_000782.1:p.Asp153=
NM_001290354.1:c.302A= NP_001277283.1:p.Asp101=
NM_001290354.2:c.302A= NP_001277283.1:p.Asp101=
NM_001290357.1:c.369+3979A= NP_001277286.1:n.369+3979A=
NM_001290357.2:c.369+3979A= NP_001277286.1:n.369+3979A=
NR_110936.1:n.773A=
NR_110936.2:n.775A=
ENST00000439211.6:c.458A= ENSP00000396308.2:p.Asp153=
ENST00000504396.1:c.302A= ENSP00000421334.1:p.Asp101=
ENST00000505337.5:c.458A= ENSP00000426474.1:p.Asp153=
ENST00000508282.1:n.416A=
ENST00000511032.5:c.369+3979A= ENSP00000422732.1:n.369+3979A=
ENST00000513048.5:n.339A=