Canonical Allele Identifier: CA3327228

Gene: DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80649381G>A , CM000667.2:g.80649381G>A	GRCh38
NC_000005.9:g.79945200G>A , CM000667.1:g.79945200G>A	GRCh37
NC_000005.8:g.79980956G>A	NCBI36
NG_023304.1:g.10601C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439211.7:c.242+8C>T MANE Select	ENSP00000396308.2:n.242+8C>T
ENST00000439211.6:c.242+8C>T	ENSP00000396308.2:n.242+8C>T
ENST00000504396.1:c.86+8C>T	ENSP00000421334.1:n.86+8C>T
ENST00000505337.5:c.242+8C>T	ENSP00000426474.1:n.242+8C>T
ENST00000508282.1:n.200+8C>T
ENST00000511032.5:c.242+8C>T	ENSP00000422732.1:n.242+8C>T
ENST00000513048.5:n.250+8C>T
ENST00000513314.1:n.142C>T
NM_000791.3:c.242+8C>T	NP_000782.1:n.242+8C>T
NM_001290354.1:c.86+8C>T	NP_001277283.1:n.86+8C>T
NM_001290357.1:c.242+8C>T	NP_001277286.1:n.242+8C>T
NR_110936.1:n.684+8C>T
NM_000791.4:c.242+8C>T MANE Select	NP_000782.1:n.242+8C>T
NM_001290354.2:c.86+8C>T	NP_001277283.1:n.86+8C>T
NM_001290357.2:c.242+8C>T	NP_001277286.1:n.242+8C>T
NR_110936.2:n.686+8C>T