Canonical Allele Identifier: CA2674438855

Gene: DHFR

Linked Data

• gnomAD v4: 5-80628993-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628993A>T , CM000667.2:g.80628993A>T	GRCh38
NC_000005.9:g.79924812A>T , CM000667.1:g.79924812A>T	GRCh37
NC_000005.8:g.79960568A>T	NCBI36
NG_023304.1:g.30989T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*94T>A MANE Select	ENSP00000396308.2:n.*94T>A
ENST00000439211.6:c.*94T>A	ENSP00000396308.2:n.*94T>A
ENST00000504396.1:c.*94T>A	ENSP00000421334.1:n.*94T>A
ENST00000505337.5:c.*48+46T>A	ENSP00000426474.1:n.*48+46T>A
ENST00000511032.5:c.*152T>A	ENSP00000422732.1:n.*152T>A
ENST00000513048.5:n.539T>A
NM_000791.3:c.*94T>A	NP_000782.1:n.*94T>A
NM_001290354.1:c.*94T>A	NP_001277283.1:n.*94T>A
NM_001290357.1:c.*152T>A	NP_001277286.1:n.*152T>A
NR_110936.1:n.973T>A
NM_000791.4:c.*94T>A MANE Select	NP_000782.1:n.*94T>A
NM_001290354.2:c.*94T>A	NP_001277283.1:n.*94T>A
NM_001290357.2:c.*152T>A	NP_001277286.1:n.*152T>A
NR_110936.2:n.975T>A