Canonical Allele Identifier: CA2674438840

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628977-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628977G>A , CM000667.2:g.80628977G>A	GRCh38
NC_000005.9:g.79924796G>A , CM000667.1:g.79924796G>A	GRCh37
NC_000005.8:g.79960552G>A	NCBI36
NG_023304.1:g.31005C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*110C>T MANE Select	ENSP00000396308.2:n.*110C>T
ENST00000439211.6:c.*110C>T	ENSP00000396308.2:n.*110C>T
ENST00000504396.1:c.*110C>T	ENSP00000421334.1:n.*110C>T
ENST00000505337.5:c.*49-39C>T	ENSP00000426474.1:n.*49-39C>T
ENST00000511032.5:c.*168C>T	ENSP00000422732.1:n.*168C>T
ENST00000513048.5:n.555C>T
NM_000791.3:c.*110C>T	NP_000782.1:n.*110C>T
NM_001290354.1:c.*110C>T	NP_001277283.1:n.*110C>T
NM_001290357.1:c.*168C>T	NP_001277286.1:n.*168C>T
NR_110936.1:n.989C>T
NM_000791.4:c.*110C>T MANE Select	NP_000782.1:n.*110C>T
NM_001290354.2:c.*110C>T	NP_001277283.1:n.*110C>T
NM_001290357.2:c.*168C>T	NP_001277286.1:n.*168C>T
NR_110936.2:n.991C>T