Canonical Allele Identifier: CA2674438773

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628891-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628891G>T , CM000667.2:g.80628891G>T	GRCh38
NC_000005.9:g.79924710G>T , CM000667.1:g.79924710G>T	GRCh37
NC_000005.8:g.79960466G>T	NCBI36
NG_023304.1:g.31091C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*196C>A MANE Select	ENSP00000396308.2:n.*196C>A
ENST00000439211.6:c.*196C>A	ENSP00000396308.2:n.*196C>A
ENST00000504396.1:c.*196C>A	ENSP00000421334.1:n.*196C>A
ENST00000505337.5:c.*96C>A	ENSP00000426474.1:n.*96C>A
ENST00000511032.5:c.*254C>A	ENSP00000422732.1:n.*254C>A
ENST00000513048.5:n.641C>A
NM_000791.3:c.*196C>A	NP_000782.1:n.*196C>A
NM_001290354.1:c.*196C>A	NP_001277283.1:n.*196C>A
NM_001290357.1:c.*254C>A	NP_001277286.1:n.*254C>A
NR_110936.1:n.1075C>A
NM_000791.4:c.*196C>A MANE Select	NP_000782.1:n.*196C>A
NM_001290354.2:c.*196C>A	NP_001277283.1:n.*196C>A
NM_001290357.2:c.*254C>A	NP_001277286.1:n.*254C>A
NR_110936.2:n.1077C>A