Canonical Allele Identifier: CA367308151
Gene: MPLKIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40173938G>C (hg19) chr7:g.40134339G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134339G>C , CM000669.2:g.40134339G>C GRCh38
NC_000007.13:g.40173938G>C , CM000669.1:g.40173938G>C GRCh37
NC_000007.12:g.40140463G>C NCBI36
NG_016989.2:g.5314C>G
NG_023422.1:g.4364G>C
NG_023422.2:g.4364G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.229C>G MANE Select ENSP00000304553.5:p.Arg77Gly
ENST00000306984.6:c.229C>G ENSP00000304553.5:p.Arg77Gly
NM_138701.3:c.229C>G NP_619646.1:p.Arg77Gly
NM_138701.4:c.229C>G MANE Select NP_619646.1:p.Arg77Gly
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Search 100 bp 3'