Canonical Allele Identifier: CA445163015

Gene: DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80653994T>C , CM000667.2:g.80653994T>C	GRCh38
NC_000005.9:g.79949813T>C , CM000667.1:g.79949813T>C	GRCh37
NC_000005.8:g.79985569T>C	NCBI36
NG_016607.1:g.4520T>C
NG_023304.1:g.5988A>G
NG_016607.2:g.4520T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.136+14A>G MANE Select	NP_000782.1:n.136+14A>G
ENST00000439211.7:c.136+14A>G MANE Select	ENSP00000396308.2:n.136+14A>G
NM_000791.3:c.136+14A>G	NP_000782.1:n.136+14A>G
NM_001290354.1:c.-21+410A>G	NP_001277283.1:n.-21+410A>G
NM_001290354.2:c.-21+410A>G	NP_001277283.1:n.-21+410A>G
NM_001290357.1:c.136+14A>G	NP_001277286.1:n.136+14A>G
NM_001290357.2:c.136+14A>G	NP_001277286.1:n.136+14A>G
NR_110936.1:n.578+410A>G
NR_110936.2:n.580+410A>G
ENST00000439211.6:c.136+14A>G	ENSP00000396308.2:n.136+14A>G
ENST00000504396.1:c.-21+410A>G	ENSP00000421334.1:n.-21+410A>G
ENST00000505337.5:c.136+14A>G	ENSP00000426474.1:n.136+14A>G
ENST00000508282.1:n.94+14A>G
ENST00000511032.5:c.136+14A>G	ENSP00000422732.1:n.136+14A>G
ENST00000513048.5:n.144+410A>G
ENST00000513314.1:n.28+14A>G