Canonical Allele Identifier: CA2426745280

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949933G= , CM000685.2:g.43949933G= GRCh38
NC_000023.10:g.43809179G= , CM000685.1:g.43809179G= GRCh37
NC_000023.9:g.43694123G= NCBI36
NG_009832.1:g.28743C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.268C= (NDP) MANE Select ENSP00000495972.1:p.Arg90=
ENST00000647044.1:c.268C= (NDP) ENSP00000495811.1:p.Arg90=
ENST00000378062.5:c.268C= (NDP) ENSP00000367301.5:p.Arg90=
ENST00000470584.1:n.312C= (NDP)
NM_000266.3:c.268C= (NDP) NP_000257.1:p.Arg90=
NR_046631.1:n.202G= (NDP-AS1)
NM_000266.4:c.268C= (NDP) MANE Select NP_000257.1:p.Arg90=