Canonical Allele Identifier: CA2674438765

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628886-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628886T>G , CM000667.2:g.80628886T>G	GRCh38
NC_000005.9:g.79924705T>G , CM000667.1:g.79924705T>G	GRCh37
NC_000005.8:g.79960461T>G	NCBI36
NG_023304.1:g.31096A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*201A>C MANE Select	ENSP00000396308.2:n.*201A>C
ENST00000439211.6:c.*201A>C	ENSP00000396308.2:n.*201A>C
ENST00000504396.1:c.*201A>C	ENSP00000421334.1:n.*201A>C
ENST00000505337.5:c.*101A>C	ENSP00000426474.1:n.*101A>C
ENST00000511032.5:c.*259A>C	ENSP00000422732.1:n.*259A>C
ENST00000513048.5:n.646A>C
NM_000791.3:c.*201A>C	NP_000782.1:n.*201A>C
NM_001290354.1:c.*201A>C	NP_001277283.1:n.*201A>C
NM_001290357.1:c.*259A>C	NP_001277286.1:n.*259A>C
NR_110936.1:n.1080A>C
NM_000791.4:c.*201A>C MANE Select	NP_000782.1:n.*201A>C
NM_001290354.2:c.*201A>C	NP_001277283.1:n.*201A>C
NM_001290357.2:c.*259A>C	NP_001277286.1:n.*259A>C
NR_110936.2:n.1082A>C