Canonical Allele Identifier: CA4229217
Gene: MPLKIP HGNC NCBI

Linked Data

ClinVar Variation Id: 1967091
ClinVar RCV Id: RCV002721782
dbSNP Id: rs748882240
ExAC: 7:40173936 C / G
gnomAD v2: 7-40173936-C-G
gnomAD v3: 7-40134337-C-G
gnomAD v4: 7-40134337-C-G
MyVariant Identifiers: chr7:g.40173936C>G (hg19) chr7:g.40134337C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134337C>G , CM000669.2:g.40134337C>G GRCh38
NC_000007.13:g.40173936C>G , CM000669.1:g.40173936C>G GRCh37
NC_000007.12:g.40140461C>G NCBI36
NG_016989.2:g.5316G>C
NG_023422.1:g.4362C>G
NG_023422.2:g.4362C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.231G>C MANE Select ENSP00000304553.5:p.Arg77=
ENST00000306984.6:c.231G>C ENSP00000304553.5:p.Arg77=
NM_138701.3:c.231G>C NP_619646.1:p.Arg77=
NM_138701.4:c.231G>C MANE Select NP_619646.1:p.Arg77=
Search 100 bp 5'
Search 100 bp 3'