Canonical Allele Identifier: CA1701803321
Gene: MPLKIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134438C= , CM000669.2:g.40134438C= GRCh38
NC_000007.13:g.40174037C= , CM000669.1:g.40174037C= GRCh37
NC_000007.12:g.40140562C= NCBI36
NG_016989.2:g.5215G=
NG_023422.1:g.4463C=
NG_023422.2:g.4463C=

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.130G= MANE Select ENSP00000304553.5:p.Gly44=
ENST00000306984.6:c.130G= ENSP00000304553.5:p.Gly44=
NM_138701.3:c.130G= NP_619646.1:p.Gly44=
NM_138701.4:c.130G= MANE Select NP_619646.1:p.Gly44=