Canonical Allele Identifier: CA1558462432

Gene: DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80628999A= , CM000667.2:g.80628999A=	GRCh38
NC_000005.9:g.79924818A= , CM000667.1:g.79924818A=	GRCh37
NC_000005.8:g.79960574A=	NCBI36
NG_023304.1:g.30983T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.*88T= MANE Select	ENSP00000396308.2:n.*88T=
ENST00000439211.6:c.*88T=	ENSP00000396308.2:n.*88T=
ENST00000504396.1:c.*88T=	ENSP00000421334.1:n.*88T=
ENST00000505337.5:c.*48+40T=	ENSP00000426474.1:n.*48+40T=
ENST00000511032.5:c.*146T=	ENSP00000422732.1:n.*146T=
ENST00000513048.5:n.533T=
NM_000791.3:c.*88T=	NP_000782.1:n.*88T=
NM_001290354.1:c.*88T=	NP_001277283.1:n.*88T=
NM_001290357.1:c.*146T=	NP_001277286.1:n.*146T=
NR_110936.1:n.967T=
NM_000791.4:c.*88T= MANE Select	NP_000782.1:n.*88T=
NM_001290354.2:c.*88T=	NP_001277283.1:n.*88T=
NM_001290357.2:c.*146T=	NP_001277286.1:n.*146T=
NR_110936.2:n.969T=