Canonical Allele Identifier: CA367308130
Gene: MPLKIP HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.233T>G MANE Select ENSP00000304553.5:p.Phe78Cys
ENST00000306984.6:c.233T>G ENSP00000304553.5:p.Phe78Cys
NM_138701.3:c.233T>G NP_619646.1:p.Phe78Cys
NM_138701.4:c.233T>G MANE Select NP_619646.1:p.Phe78Cys