Canonical Allele Identifier: CA917988590
Gene: MPLKIP HGNC NCBI

Linked Data

dbSNP Id: rs1562783546

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134435_40134436dup , CM000669.2:g.40134435_40134436dup GRCh38
NC_000007.13:g.40174034_40174035dup , CM000669.1:g.40174034_40174035dup GRCh37
NC_000007.12:g.40140559_40140560dup NCBI36
NG_016989.2:g.5217_5218dup
NG_023422.1:g.4460_4461dup
NG_023422.2:g.4460_4461dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.132_133dup MANE Select ENSP00000304553.5:p.Tyr45CysfsTer?
ENST00000306984.6:c.132_133dup ENSP00000304553.5:p.Tyr45CysfsTer?
NM_138701.3:c.132_133dup NP_619646.1:p.Tyr45CysfsTer?
NM_138701.4:c.132_133dup MANE Select NP_619646.1:p.Tyr45CysfsTer?