Canonical Allele Identifier: CA1701803315
Gene: MPLKIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134431C= , CM000669.2:g.40134431C= GRCh38
NC_000007.13:g.40174030C= , CM000669.1:g.40174030C= GRCh37
NC_000007.12:g.40140555C= NCBI36
NG_016989.2:g.5222G=
NG_023422.1:g.4456C=
NG_023422.2:g.4456C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.137G= MANE Select ENSP00000304553.5:p.Gly46=
ENST00000306984.6:c.137G= ENSP00000304553.5:p.Gly46=
NM_138701.3:c.137G= NP_619646.1:p.Gly46=
NM_138701.4:c.137G= MANE Select NP_619646.1:p.Gly46=