Canonical Allele Identifier: CA367308126
Gene: MPLKIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134333C>G , CM000669.2:g.40134333C>G GRCh38
NC_000007.13:g.40173932C>G , CM000669.1:g.40173932C>G GRCh37
NC_000007.12:g.40140457C>G NCBI36
NG_016989.2:g.5320G>C
NG_023422.1:g.4358C>G
NG_023422.2:g.4358C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.235G>C MANE Select ENSP00000304553.5:p.Gly79Arg
ENST00000306984.6:c.235G>C ENSP00000304553.5:p.Gly79Arg
NM_138701.3:c.235G>C NP_619646.1:p.Gly79Arg
NM_138701.4:c.235G>C MANE Select NP_619646.1:p.Gly79Arg