Canonical Allele Identifier: CA1077963473

Gene: DHFR

Linked Data

• gnomAD v3: 5-80629003-T-A
• gnomAD v4: 5-80629003-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80629003T>A , CM000667.2:g.80629003T>A	GRCh38
NC_000005.9:g.79924822T>A , CM000667.1:g.79924822T>A	GRCh37
NC_000005.8:g.79960578T>A	NCBI36
NG_023304.1:g.30979A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*84A>T MANE Select	ENSP00000396308.2:n.*84A>T
ENST00000439211.6:c.*84A>T	ENSP00000396308.2:n.*84A>T
ENST00000504396.1:c.*84A>T	ENSP00000421334.1:n.*84A>T
ENST00000505337.5:c.*48+36A>T	ENSP00000426474.1:n.*48+36A>T
ENST00000511032.5:c.*142A>T	ENSP00000422732.1:n.*142A>T
ENST00000513048.5:n.529A>T
NM_000791.3:c.*84A>T	NP_000782.1:n.*84A>T
NM_001290354.1:c.*84A>T	NP_001277283.1:n.*84A>T
NM_001290357.1:c.*142A>T	NP_001277286.1:n.*142A>T
NR_110936.1:n.963A>T
NM_000791.4:c.*84A>T MANE Select	NP_000782.1:n.*84A>T
NM_001290354.2:c.*84A>T	NP_001277283.1:n.*84A>T
NM_001290357.2:c.*142A>T	NP_001277286.1:n.*142A>T
NR_110936.2:n.965A>T