Canonical Allele Identifier: CA367308581
Gene: MPLKIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134437C>T , CM000669.2:g.40134437C>T GRCh38
NC_000007.13:g.40174036C>T , CM000669.1:g.40174036C>T GRCh37
NC_000007.12:g.40140561C>T NCBI36
NG_016989.2:g.5216G>A
NG_023422.1:g.4462C>T
NG_023422.2:g.4462C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.131G>A MANE Select ENSP00000304553.5:p.Gly44Glu
ENST00000306984.6:c.131G>A ENSP00000304553.5:p.Gly44Glu
NM_138701.3:c.131G>A NP_619646.1:p.Gly44Glu
NM_138701.4:c.131G>A MANE Select NP_619646.1:p.Gly44Glu