Canonical Allele Identifier: CA454825314
Gene: MPLKIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40174041T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134442T>C , CM000669.2:g.40134442T>C GRCh38
NC_000007.13:g.40174041T>C , CM000669.1:g.40174041T>C GRCh37
NC_000007.12:g.40140566T>C NCBI36
NG_016989.2:g.5211A>G
NG_023422.1:g.4467T>C
NG_023422.2:g.4467T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.126A>G MANE Select ENSP00000304553.5:p.Arg42=
ENST00000306984.6:c.126A>G ENSP00000304553.5:p.Arg42=
NM_138701.3:c.126A>G NP_619646.1:p.Arg42=
NM_138701.4:c.126A>G MANE Select NP_619646.1:p.Arg42=