Canonical Allele Identifier: CA367308593
Gene: MPLKIP HGNC NCBI

Linked Data

dbSNP Id: rs1433737117
gnomAD v4: 7-40134440-T-C
MyVariant Identifiers: chr7:g.40174039T>C (hg19) chr7:g.40134440T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134440T>C , CM000669.2:g.40134440T>C GRCh38
NC_000007.13:g.40174039T>C , CM000669.1:g.40174039T>C GRCh37
NC_000007.12:g.40140564T>C NCBI36
NG_016989.2:g.5213A>G
NG_023422.1:g.4465T>C
NG_023422.2:g.4465T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.128A>G MANE Select ENSP00000304553.5:p.Asp43Gly
ENST00000306984.6:c.128A>G ENSP00000304553.5:p.Asp43Gly
NM_138701.3:c.128A>G NP_619646.1:p.Asp43Gly
NM_138701.4:c.128A>G MANE Select NP_619646.1:p.Asp43Gly
Search 100 bp 5'
Search 100 bp 3'