Canonical Allele Identifier: CA367308133
Gene: MPLKIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134335A>T , CM000669.2:g.40134335A>T GRCh38
NC_000007.13:g.40173934A>T , CM000669.1:g.40173934A>T GRCh37
NC_000007.12:g.40140459A>T NCBI36
NG_016989.2:g.5318T>A
NG_023422.1:g.4360A>T
NG_023422.2:g.4360A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.233T>A MANE Select ENSP00000304553.5:p.Phe78Tyr
ENST00000306984.6:c.233T>A ENSP00000304553.5:p.Phe78Tyr
NM_138701.3:c.233T>A NP_619646.1:p.Phe78Tyr
NM_138701.4:c.233T>A MANE Select NP_619646.1:p.Phe78Tyr