Canonical Allele Identifier: CA1701803243
Gene: MPLKIP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134337C= , CM000669.2:g.40134337C= GRCh38
NC_000007.13:g.40173936C= , CM000669.1:g.40173936C= GRCh37
NC_000007.12:g.40140461C= NCBI36
NG_016989.2:g.5316G=
NG_023422.1:g.4362C=
NG_023422.2:g.4362C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.231G= MANE Select ENSP00000304553.5:p.Arg77=
ENST00000306984.6:c.231G= ENSP00000304553.5:p.Arg77=
NM_138701.3:c.231G= NP_619646.1:p.Arg77=
NM_138701.4:c.231G= MANE Select NP_619646.1:p.Arg77=