Canonical Allele Identifier: CA367308602
Gene: MPLKIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40174040C>T (hg19) chr7:g.40134441C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134441C>T , CM000669.2:g.40134441C>T GRCh38
NC_000007.13:g.40174040C>T , CM000669.1:g.40174040C>T GRCh37
NC_000007.12:g.40140565C>T NCBI36
NG_016989.2:g.5212G>A
NG_023422.1:g.4466C>T
NG_023422.2:g.4466C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.127G>A MANE Select ENSP00000304553.5:p.Asp43Asn
ENST00000306984.6:c.127G>A ENSP00000304553.5:p.Asp43Asn
NM_138701.3:c.127G>A NP_619646.1:p.Asp43Asn
NM_138701.4:c.127G>A MANE Select NP_619646.1:p.Asp43Asn
Search 100 bp 5'
Search 100 bp 3'