Canonical Allele Identifier: CA1701803242
Gene: MPLKIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134334G= , CM000669.2:g.40134334G= GRCh38
NC_000007.13:g.40173933G= , CM000669.1:g.40173933G= GRCh37
NC_000007.12:g.40140458G= NCBI36
NG_016989.2:g.5319C=
NG_023422.1:g.4359G=
NG_023422.2:g.4359G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.234C= MANE Select ENSP00000304553.5:p.Phe78=
ENST00000306984.6:c.234C= ENSP00000304553.5:p.Phe78=
NM_138701.3:c.234C= NP_619646.1:p.Phe78=
NM_138701.4:c.234C= MANE Select NP_619646.1:p.Phe78=