Canonical Allele Identifier: CA454825169
Gene: MPLKIP HGNC NCBI

Linked Data

gnomAD v4: 7-40134340-G-T
MyVariant Identifiers: chr7:g.40173939G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134340G>T , CM000669.2:g.40134340G>T GRCh38
NC_000007.13:g.40173939G>T , CM000669.1:g.40173939G>T GRCh37
NC_000007.12:g.40140464G>T NCBI36
NG_016989.2:g.5313C>A
NG_023422.1:g.4365G>T
NG_023422.2:g.4365G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.228C>A MANE Select ENSP00000304553.5:p.Gly76=
ENST00000306984.6:c.228C>A ENSP00000304553.5:p.Gly76=
NM_138701.3:c.228C>A NP_619646.1:p.Gly76=
NM_138701.4:c.228C>A MANE Select NP_619646.1:p.Gly76=
Search 100 bp 5'
Search 100 bp 3'