Canonical Allele Identifier: CA2674438850

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628988-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628988A>G , CM000667.2:g.80628988A>G	GRCh38
NC_000005.9:g.79924807A>G , CM000667.1:g.79924807A>G	GRCh37
NC_000005.8:g.79960563A>G	NCBI36
NG_023304.1:g.30994T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*99T>C MANE Select	ENSP00000396308.2:n.*99T>C
ENST00000439211.6:c.*99T>C	ENSP00000396308.2:n.*99T>C
ENST00000504396.1:c.*99T>C	ENSP00000421334.1:n.*99T>C
ENST00000505337.5:c.*49-50T>C	ENSP00000426474.1:n.*49-50T>C
ENST00000511032.5:c.*157T>C	ENSP00000422732.1:n.*157T>C
ENST00000513048.5:n.544T>C
NM_000791.3:c.*99T>C	NP_000782.1:n.*99T>C
NM_001290354.1:c.*99T>C	NP_001277283.1:n.*99T>C
NM_001290357.1:c.*157T>C	NP_001277286.1:n.*157T>C
NR_110936.1:n.978T>C
NM_000791.4:c.*99T>C MANE Select	NP_000782.1:n.*99T>C
NM_001290354.2:c.*99T>C	NP_001277283.1:n.*99T>C
NM_001290357.2:c.*157T>C	NP_001277286.1:n.*157T>C
NR_110936.2:n.980T>C