Canonical Allele Identifier: CA2426745251

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949853G= , CM000685.2:g.43949853G= GRCh38
NC_000023.10:g.43809099G= , CM000685.1:g.43809099G= GRCh37
NC_000023.9:g.43694043G= NCBI36
NG_009832.1:g.28823C=

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.348C= (NDP) MANE Select ENSP00000495972.1:p.Leu116=
ENST00000647044.1:c.348C= (NDP) ENSP00000495811.1:p.Leu116=
ENST00000378062.5:c.348C= (NDP) ENSP00000367301.5:p.Leu116=
ENST00000470584.1:n.392C= (NDP)
NM_000266.3:c.348C= (NDP) NP_000257.1:p.Leu116=
NR_046631.1:n.122G= (NDP-AS1)
NM_000266.4:c.348C= (NDP) MANE Select NP_000257.1:p.Leu116=