Canonical Allele Identifier: CA1701803317
Gene: MPLKIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134433G= , CM000669.2:g.40134433G= GRCh38
NC_000007.13:g.40174032G= , CM000669.1:g.40174032G= GRCh37
NC_000007.12:g.40140557G= NCBI36
NG_016989.2:g.5220C=
NG_023422.1:g.4458G=
NG_023422.2:g.4458G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.135C= MANE Select ENSP00000304553.5:p.Tyr45=
ENST00000306984.6:c.135C= ENSP00000304553.5:p.Tyr45=
NM_138701.3:c.135C= NP_619646.1:p.Tyr45=
NM_138701.4:c.135C= MANE Select NP_619646.1:p.Tyr45=