Canonical Allele Identifier: CA367308561
Gene: MPLKIP HGNC NCBI

Linked Data

gnomAD v4: 7-40134433-G-T
MyVariant Identifiers: chr7:g.40174032G>T (hg19) chr7:g.40134433G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134433G>T , CM000669.2:g.40134433G>T GRCh38
NC_000007.13:g.40174032G>T , CM000669.1:g.40174032G>T GRCh37
NC_000007.12:g.40140557G>T NCBI36
NG_016989.2:g.5220C>A
NG_023422.1:g.4458G>T
NG_023422.2:g.4458G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000306984.8:c.135C>A MANE Select ENSP00000304553.5:p.Tyr45Ter
ENST00000306984.6:c.135C>A ENSP00000304553.5:p.Tyr45Ter
NM_138701.3:c.135C>A NP_619646.1:p.Tyr45Ter
NM_138701.4:c.135C>A MANE Select NP_619646.1:p.Tyr45Ter
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