Canonical Allele Identifier: CA4229216
Gene: MPLKIP HGNC NCBI

Linked Data

ClinVar Variation Id: 2963025
ClinVar RCV Id: RCV003828135
dbSNP Id: rs775282020
ExAC: 7:40173933 G / A
gnomAD v2: 7-40173933-G-A
gnomAD v3: 7-40134334-G-A
gnomAD v4: 7-40134334-G-A
MyVariant Identifiers: chr7:g.40173933G>A (hg19) chr7:g.40134334G>A (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.234C>T MANE Select ENSP00000304553.5:p.Phe78=
ENST00000306984.6:c.234C>T ENSP00000304553.5:p.Phe78=
NM_138701.3:c.234C>T NP_619646.1:p.Phe78=
NM_138701.4:c.234C>T MANE Select NP_619646.1:p.Phe78=
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Search 100 bp 3'