Canonical Allele Identifier: CA367308154
Gene: MPLKIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2099442
ClinVar RCV Id: RCV003021727
MyVariant Identifiers: chr7:g.40173940C>T (hg19) chr7:g.40134341C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134341C>T , CM000669.2:g.40134341C>T GRCh38
NC_000007.13:g.40173940C>T , CM000669.1:g.40173940C>T GRCh37
NC_000007.12:g.40140465C>T NCBI36
NG_016989.2:g.5312G>A
NG_023422.1:g.4366C>T
NG_023422.2:g.4366C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.227G>A MANE Select ENSP00000304553.5:p.Gly76Asp
ENST00000306984.6:c.227G>A ENSP00000304553.5:p.Gly76Asp
NM_138701.3:c.227G>A NP_619646.1:p.Gly76Asp
NM_138701.4:c.227G>A MANE Select NP_619646.1:p.Gly76Asp
Search 100 bp 5'
Search 100 bp 3'