Canonical Allele Identifier: CA2426745258

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949873A= , CM000685.2:g.43949873A= GRCh38
NC_000023.10:g.43809119A= , CM000685.1:g.43809119A= GRCh37
NC_000023.9:g.43694063A= NCBI36
NG_009832.1:g.28803T=

Transcript Alleles

HGVS Amino-acid change
ENST00000642620.1:c.328T= (NDP) MANE Select ENSP00000495972.1:p.Cys110=
ENST00000647044.1:c.328T= (NDP) ENSP00000495811.1:p.Cys110=
ENST00000378062.5:c.328T= (NDP) ENSP00000367301.5:p.Cys110=
ENST00000470584.1:n.372T= (NDP)
NM_000266.3:c.328T= (NDP) NP_000257.1:p.Cys110=
NR_046631.1:n.142A= (NDP-AS1)
NM_000266.4:c.328T= (NDP) MANE Select NP_000257.1:p.Cys110=