Canonical Allele Identifier: CA2674438755

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628876-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628876G>A , CM000667.2:g.80628876G>A	GRCh38
NC_000005.9:g.79924695G>A , CM000667.1:g.79924695G>A	GRCh37
NC_000005.8:g.79960451G>A	NCBI36
NG_023304.1:g.31106C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*211C>T MANE Select	ENSP00000396308.2:n.*211C>T
ENST00000439211.6:c.*211C>T	ENSP00000396308.2:n.*211C>T
ENST00000504396.1:c.*211C>T	ENSP00000421334.1:n.*211C>T
ENST00000505337.5:c.*111C>T	ENSP00000426474.1:n.*111C>T
ENST00000511032.5:c.*269C>T	ENSP00000422732.1:n.*269C>T
ENST00000513048.5:n.656C>T
NM_000791.3:c.*211C>T	NP_000782.1:n.*211C>T
NM_001290354.1:c.*211C>T	NP_001277283.1:n.*211C>T
NM_001290357.1:c.*269C>T	NP_001277286.1:n.*269C>T
NR_110936.1:n.1090C>T
NM_000791.4:c.*211C>T MANE Select	NP_000782.1:n.*211C>T
NM_001290354.2:c.*211C>T	NP_001277283.1:n.*211C>T
NM_001290357.2:c.*269C>T	NP_001277286.1:n.*269C>T
NR_110936.2:n.1092C>T