Canonical Allele Identifier: CA454825159
Gene: MPLKIP HGNC NCBI

Linked Data

gnomAD v4: 7-40134331-C-G
MyVariant Identifiers: chr7:g.40173930C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134331C>G , CM000669.2:g.40134331C>G GRCh38
NC_000007.13:g.40173930C>G , CM000669.1:g.40173930C>G GRCh37
NC_000007.12:g.40140455C>G NCBI36
NG_016989.2:g.5322G>C
NG_023422.1:g.4356C>G
NG_023422.2:g.4356C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.237G>C MANE Select ENSP00000304553.5:p.Gly79=
ENST00000306984.6:c.237G>C ENSP00000304553.5:p.Gly79=
NM_138701.3:c.237G>C NP_619646.1:p.Gly79=
NM_138701.4:c.237G>C MANE Select NP_619646.1:p.Gly79=