Canonical Allele Identifier: CA1701803323
Gene: MPLKIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134441C= , CM000669.2:g.40134441C= GRCh38
NC_000007.13:g.40174040C= , CM000669.1:g.40174040C= GRCh37
NC_000007.12:g.40140565C= NCBI36
NG_016989.2:g.5212G=
NG_023422.1:g.4466C=
NG_023422.2:g.4466C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.127G= MANE Select ENSP00000304553.5:p.Asp43=
ENST00000306984.6:c.127G= ENSP00000304553.5:p.Asp43=
NM_138701.3:c.127G= NP_619646.1:p.Asp43=
NM_138701.4:c.127G= MANE Select NP_619646.1:p.Asp43=