Canonical Allele Identifier: CA454825313
Gene: MPLKIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40174041T>A (hg19)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.126A>T MANE Select ENSP00000304553.5:p.Arg42=
ENST00000306984.6:c.126A>T ENSP00000304553.5:p.Arg42=
NM_138701.3:c.126A>T NP_619646.1:p.Arg42=
NM_138701.4:c.126A>T MANE Select NP_619646.1:p.Arg42=
Search 100 bp 5'
Search 100 bp 3'