Canonical Allele Identifier: CA2674438845

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628979-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628979T>C , CM000667.2:g.80628979T>C	GRCh38
NC_000005.9:g.79924798T>C , CM000667.1:g.79924798T>C	GRCh37
NC_000005.8:g.79960554T>C	NCBI36
NG_023304.1:g.31003A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*108A>G MANE Select	ENSP00000396308.2:n.*108A>G
ENST00000439211.6:c.*108A>G	ENSP00000396308.2:n.*108A>G
ENST00000504396.1:c.*108A>G	ENSP00000421334.1:n.*108A>G
ENST00000505337.5:c.*49-41A>G	ENSP00000426474.1:n.*49-41A>G
ENST00000511032.5:c.*166A>G	ENSP00000422732.1:n.*166A>G
ENST00000513048.5:n.553A>G
NM_000791.3:c.*108A>G	NP_000782.1:n.*108A>G
NM_001290354.1:c.*108A>G	NP_001277283.1:n.*108A>G
NM_001290357.1:c.*166A>G	NP_001277286.1:n.*166A>G
NR_110936.1:n.987A>G
NM_000791.4:c.*108A>G MANE Select	NP_000782.1:n.*108A>G
NM_001290354.2:c.*108A>G	NP_001277283.1:n.*108A>G
NM_001290357.2:c.*166A>G	NP_001277286.1:n.*166A>G
NR_110936.2:n.989A>G