Canonical Allele Identifier: CA413007660

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.43949944T>G , CM000685.2:g.43949944T>G GRCh38
NC_000023.10:g.43809190T>G , CM000685.1:g.43809190T>G GRCh37
NC_000023.9:g.43694134T>G NCBI36
NG_009832.1:g.28732A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000642620.1:c.257A>C (NDP) MANE Select ENSP00000495972.1:p.Lys86Thr
ENST00000647044.1:c.257A>C (NDP) ENSP00000495811.1:p.Lys86Thr
ENST00000378062.5:c.257A>C (NDP) ENSP00000367301.5:p.Lys86Thr
ENST00000470584.1:n.301A>C (NDP)
NM_000266.3:c.257A>C (NDP) NP_000257.1:p.Lys86Thr
NR_046631.1:n.213T>G (NDP-AS1)
NM_000266.4:c.257A>C (NDP) MANE Select NP_000257.1:p.Lys86Thr