Canonical Allele Identifier: CA2674438858

Gene: DHFR

Linked Data

• gnomAD v4: 5-80629000-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80629000A>C , CM000667.2:g.80629000A>C	GRCh38
NC_000005.9:g.79924819A>C , CM000667.1:g.79924819A>C	GRCh37
NC_000005.8:g.79960575A>C	NCBI36
NG_023304.1:g.30982T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*87T>G MANE Select	ENSP00000396308.2:n.*87T>G
ENST00000439211.6:c.*87T>G	ENSP00000396308.2:n.*87T>G
ENST00000504396.1:c.*87T>G	ENSP00000421334.1:n.*87T>G
ENST00000505337.5:c.*48+39T>G	ENSP00000426474.1:n.*48+39T>G
ENST00000511032.5:c.*145T>G	ENSP00000422732.1:n.*145T>G
ENST00000513048.5:n.532T>G
NM_000791.3:c.*87T>G	NP_000782.1:n.*87T>G
NM_001290354.1:c.*87T>G	NP_001277283.1:n.*87T>G
NM_001290357.1:c.*145T>G	NP_001277286.1:n.*145T>G
NR_110936.1:n.966T>G
NM_000791.4:c.*87T>G MANE Select	NP_000782.1:n.*87T>G
NM_001290354.2:c.*87T>G	NP_001277283.1:n.*87T>G
NM_001290357.2:c.*145T>G	NP_001277286.1:n.*145T>G
NR_110936.2:n.968T>G