Canonical Allele Identifier: CA367308138
Gene: MPLKIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40173935A>T (hg19) chr7:g.40134336A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134336A>T , CM000669.2:g.40134336A>T GRCh38
NC_000007.13:g.40173935A>T , CM000669.1:g.40173935A>T GRCh37
NC_000007.12:g.40140460A>T NCBI36
NG_016989.2:g.5317T>A
NG_023422.1:g.4361A>T
NG_023422.2:g.4361A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.232T>A MANE Select ENSP00000304553.5:p.Phe78Ile
ENST00000306984.6:c.232T>A ENSP00000304553.5:p.Phe78Ile
NM_138701.3:c.232T>A NP_619646.1:p.Phe78Ile
NM_138701.4:c.232T>A MANE Select NP_619646.1:p.Phe78Ile
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