Canonical Allele Identifier: CA4229233
Gene: MPLKIP HGNC NCBI

Linked Data

dbSNP Id: rs750370923
ExAC: 7:40174035 C / G
gnomAD v2: 7-40174035-C-G
gnomAD v4: 7-40134436-C-G
MyVariant Identifiers: chr7:g.40174035C>G (hg19) chr7:g.40134436C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.132G>C MANE Select ENSP00000304553.5:p.Gly44=
ENST00000306984.6:c.132G>C ENSP00000304553.5:p.Gly44=
NM_138701.3:c.132G>C NP_619646.1:p.Gly44=
NM_138701.4:c.132G>C MANE Select NP_619646.1:p.Gly44=
Search 100 bp 5'
Search 100 bp 3'