Canonical Allele Identifier: CA2674438754

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628875-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628879del , CM000667.2:g.80628879del	GRCh38
NC_000005.9:g.79924698del , CM000667.1:g.79924698del	GRCh37
NC_000005.8:g.79960454del	NCBI36
NG_023304.1:g.31106del

Transcript Alleles

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