Canonical Allele Identifier: CA1558476203

Gene: DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80643456A= , CM000667.2:g.80643456A=	GRCh38
NC_000005.9:g.79939275A= , CM000667.1:g.79939275A=	GRCh37
NC_000005.8:g.79975031A=	NCBI36
NG_023304.1:g.16526T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.243-5447T= MANE Select	ENSP00000396308.2:n.243-5447T=
ENST00000439211.6:c.243-5447T=	ENSP00000396308.2:n.243-5447T=
ENST00000504396.1:c.87-5447T=	ENSP00000421334.1:n.87-5447T=
ENST00000505337.5:c.243-5447T=	ENSP00000426474.1:n.243-5447T=
ENST00000508282.1:n.201-5447T=
ENST00000511032.5:c.243-5447T=	ENSP00000422732.1:n.243-5447T=
ENST00000513048.5:n.250+5933T=
NM_000791.3:c.243-5447T=	NP_000782.1:n.243-5447T=
NM_001290354.1:c.87-5447T=	NP_001277283.1:n.87-5447T=
NM_001290357.1:c.243-5447T=	NP_001277286.1:n.243-5447T=
NR_110936.1:n.684+5933T=
NM_000791.4:c.243-5447T= MANE Select	NP_000782.1:n.243-5447T=
NM_001290354.2:c.87-5447T=	NP_001277283.1:n.87-5447T=
NM_001290357.2:c.243-5447T=	NP_001277286.1:n.243-5447T=
NR_110936.2:n.686+5933T=