Canonical Allele Identifier: CA445162583
Community Standard Title: NM_000791.4(DHFR):c.201T>C (p.Pro67=)
Gene: DHFR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.80649430A>G , CM000667.2:g.80649430A>G GRCh38
NC_000005.9:g.79945249A>G , CM000667.1:g.79945249A>G GRCh37
NC_000005.8:g.79981005A>G NCBI36
NG_023304.1:g.10552T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000791.4:c.201T>C MANE Select NP_000782.1:p.Pro67=
ENST00000439211.7:c.201T>C MANE Select ENSP00000396308.2:p.Pro67=
NM_000791.3:c.201T>C NP_000782.1:p.Pro67=
NM_001290354.1:c.45T>C NP_001277283.1:p.Pro15=
NM_001290354.2:c.45T>C NP_001277283.1:p.Pro15=
NM_001290357.1:c.201T>C NP_001277286.1:p.Pro67=
NM_001290357.2:c.201T>C NP_001277286.1:p.Pro67=
NR_110936.1:n.643T>C
NR_110936.2:n.645T>C
ENST00000439211.6:c.201T>C ENSP00000396308.2:p.Pro67=
ENST00000504396.1:c.45T>C ENSP00000421334.1:p.Pro15=
ENST00000505337.5:c.201T>C ENSP00000426474.1:p.Pro67=
ENST00000508282.1:n.159T>C
ENST00000511032.5:c.201T>C ENSP00000422732.1:p.Pro67=
ENST00000513048.5:n.209T>C
ENST00000513314.1:n.93T>C