Canonical Allele Identifier: CA413007423

Linked Data

COSMIC: COSM757247

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949881C>A , CM000685.2:g.43949881C>A GRCh38
NC_000023.10:g.43809127C>A , CM000685.1:g.43809127C>A GRCh37
NC_000023.9:g.43694071C>A NCBI36
NG_009832.1:g.28795G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.320G>T (NDP) MANE Select ENSP00000495972.1:p.Arg107Leu
ENST00000647044.1:c.320G>T (NDP) ENSP00000495811.1:p.Arg107Leu
ENST00000378062.5:c.320G>T (NDP) ENSP00000367301.5:p.Arg107Leu
ENST00000470584.1:n.364G>T (NDP)
NM_000266.3:c.320G>T (NDP) NP_000257.1:p.Arg107Leu
NR_046631.1:n.150C>A (NDP-AS1)
NM_000266.4:c.320G>T (NDP) MANE Select NP_000257.1:p.Arg107Leu