Canonical Allele Identifier: CA367308567
Gene: MPLKIP HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.40174033T>G (hg19) chr7:g.40134434T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134434T>G , CM000669.2:g.40134434T>G GRCh38
NC_000007.13:g.40174033T>G , CM000669.1:g.40174033T>G GRCh37
NC_000007.12:g.40140558T>G NCBI36
NG_016989.2:g.5219A>C
NG_023422.1:g.4459T>G
NG_023422.2:g.4459T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.134A>C MANE Select ENSP00000304553.5:p.Tyr45Ser
ENST00000306984.6:c.134A>C ENSP00000304553.5:p.Tyr45Ser
NM_138701.3:c.134A>C NP_619646.1:p.Tyr45Ser
NM_138701.4:c.134A>C MANE Select NP_619646.1:p.Tyr45Ser
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Search 100 bp 3'