Canonical Allele Identifier: CA2674438767

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628887-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628891del , CM000667.2:g.80628891del	GRCh38
NC_000005.9:g.79924710del , CM000667.1:g.79924710del	GRCh37
NC_000005.8:g.79960466del	NCBI36
NG_023304.1:g.31094del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*199del MANE Select	ENSP00000396308.2:n.*199del
ENST00000439211.6:c.*199del	ENSP00000396308.2:n.*199del
ENST00000504396.1:c.*199del	ENSP00000421334.1:n.*199del
ENST00000505337.5:c.*99del	ENSP00000426474.1:n.*99del
ENST00000511032.5:c.*257del	ENSP00000422732.1:n.*257del
ENST00000513048.5:n.644del
NM_000791.3:c.*199del	NP_000782.1:n.*199del
NM_001290354.1:c.*199del	NP_001277283.1:n.*199del
NM_001290357.1:c.*257del	NP_001277286.1:n.*257del
NR_110936.1:n.1078del
NM_000791.4:c.*199del MANE Select	NP_000782.1:n.*199del
NM_001290354.2:c.*199del	NP_001277283.1:n.*199del
NM_001290357.2:c.*257del	NP_001277286.1:n.*257del
NR_110936.2:n.1080del