Canonical Allele Identifier: CA2674438762

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628883-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628883C>T , CM000667.2:g.80628883C>T	GRCh38
NC_000005.9:g.79924702C>T , CM000667.1:g.79924702C>T	GRCh37
NC_000005.8:g.79960458C>T	NCBI36
NG_023304.1:g.31099G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*204G>A MANE Select	ENSP00000396308.2:n.*204G>A
ENST00000439211.6:c.*204G>A	ENSP00000396308.2:n.*204G>A
ENST00000504396.1:c.*204G>A	ENSP00000421334.1:n.*204G>A
ENST00000505337.5:c.*104G>A	ENSP00000426474.1:n.*104G>A
ENST00000511032.5:c.*262G>A	ENSP00000422732.1:n.*262G>A
ENST00000513048.5:n.649G>A
NM_000791.3:c.*204G>A	NP_000782.1:n.*204G>A
NM_001290354.1:c.*204G>A	NP_001277283.1:n.*204G>A
NM_001290357.1:c.*262G>A	NP_001277286.1:n.*262G>A
NR_110936.1:n.1083G>A
NM_000791.4:c.*204G>A MANE Select	NP_000782.1:n.*204G>A
NM_001290354.2:c.*204G>A	NP_001277283.1:n.*204G>A
NM_001290357.2:c.*262G>A	NP_001277286.1:n.*262G>A
NR_110936.2:n.1085G>A