Canonical Allele Identifier: CA157713277
Gene: MPLKIP HGNC NCBI

Linked Data

ClinVar Variation Id: 734605
ClinVar RCV Id: RCV000910047
dbSNP Id: rs980652263
gnomAD v2: 7-40174041-T-G
gnomAD v3: 7-40134442-T-G
gnomAD v4: 7-40134442-T-G
MyVariant Identifiers: chr7:g.40174041T>G (hg19) chr7:g.40134442T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134442T>G , CM000669.2:g.40134442T>G GRCh38
NC_000007.13:g.40174041T>G , CM000669.1:g.40174041T>G GRCh37
NC_000007.12:g.40140566T>G NCBI36
NG_016989.2:g.5211A>C
NG_023422.1:g.4467T>G
NG_023422.2:g.4467T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.126A>C MANE Select ENSP00000304553.5:p.Arg42=
ENST00000306984.6:c.126A>C ENSP00000304553.5:p.Arg42=
NM_138701.3:c.126A>C NP_619646.1:p.Arg42=
NM_138701.4:c.126A>C MANE Select NP_619646.1:p.Arg42=
Search 100 bp 5'
Search 100 bp 3'