Canonical Allele Identifier: CA1701803322
Gene: MPLKIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134440T= , CM000669.2:g.40134440T= GRCh38
NC_000007.13:g.40174039T= , CM000669.1:g.40174039T= GRCh37
NC_000007.12:g.40140564T= NCBI36
NG_016989.2:g.5213A=
NG_023422.1:g.4465T=
NG_023422.2:g.4465T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.128A= MANE Select ENSP00000304553.5:p.Asp43=
ENST00000306984.6:c.128A= ENSP00000304553.5:p.Asp43=
NM_138701.3:c.128A= NP_619646.1:p.Asp43=
NM_138701.4:c.128A= MANE Select NP_619646.1:p.Asp43=