Canonical Allele Identifier: CA454825310
Gene: MPLKIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40174035C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134436C>A , CM000669.2:g.40134436C>A GRCh38
NC_000007.13:g.40174035C>A , CM000669.1:g.40174035C>A GRCh37
NC_000007.12:g.40140560C>A NCBI36
NG_016989.2:g.5217G>T
NG_023422.1:g.4461C>A
NG_023422.2:g.4461C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.132G>T MANE Select ENSP00000304553.5:p.Gly44=
ENST00000306984.6:c.132G>T ENSP00000304553.5:p.Gly44=
NM_138701.3:c.132G>T NP_619646.1:p.Gly44=
NM_138701.4:c.132G>T MANE Select NP_619646.1:p.Gly44=