Canonical Allele Identifier: CA2674439549

Gene: DHFR

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.80634013_80634019del , CM000667.2:g.80634013_80634019del	GRCh38
NC_000005.9:g.79929832_79929838del , CM000667.1:g.79929832_79929838del	GRCh37
NC_000005.8:g.79965588_79965594del	NCBI36
NG_023304.1:g.25965_25971del

Transcript Alleles

HGVS	Amino-acid Change
NM_000791.4:c.370-25_370-19del MANE Select	NP_000782.1:n.370-25_370-19del
ENST00000439211.7:c.370-25_370-19del MANE Select	ENSP00000396308.2:n.370-25_370-19del
NM_000791.3:c.370-25_370-19del	NP_000782.1:n.370-25_370-19del
NM_001290354.1:c.214-25_214-19del	NP_001277283.1:n.214-25_214-19del
NM_001290354.2:c.214-25_214-19del	NP_001277283.1:n.214-25_214-19del
NM_001290357.1:c.369+3866_369+3872del	NP_001277286.1:n.369+3866_369+3872del
NM_001290357.2:c.369+3866_369+3872del	NP_001277286.1:n.369+3866_369+3872del
NR_110936.1:n.685-25_685-19del
NR_110936.2:n.687-25_687-19del
ENST00000439211.6:c.370-25_370-19del	ENSP00000396308.2:n.370-25_370-19del
ENST00000504396.1:c.214-25_214-19del	ENSP00000421334.1:n.214-25_214-19del
ENST00000505337.5:c.370-25_370-19del	ENSP00000426474.1:n.370-25_370-19del
ENST00000508282.1:n.328-25_328-19del
ENST00000511032.5:c.369+3866_369+3872del	ENSP00000422732.1:n.369+3866_369+3872del
ENST00000513048.5:n.251-25_251-19del