Canonical Allele Identifier: CA574231002
Gene: MPLKIP HGNC NCBI

Linked Data

dbSNP Id: rs1562783168
gnomAD v2: 7-40173939-GC-G
gnomAD v3: 7-40134340-GC-G
gnomAD v4: 7-40134340-GC-G
MyVariant Identifiers: chr7:g.40173940del (hg19) chr7:g.40134341del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.40134346del , CM000669.2:g.40134346del GRCh38
NC_000007.13:g.40173945del , CM000669.1:g.40173945del GRCh37
NC_000007.12:g.40140470del NCBI36
NG_016989.2:g.5312del
NG_023422.1:g.4371del
NG_023422.2:g.4371del

Transcript Alleles

HGVS Amino-acid Change
ENST00000306984.8:c.227del MANE Select ENSP00000304553.5:p.Gly76AlafsTer?
ENST00000306984.6:c.227del ENSP00000304553.5:p.Gly76AlafsTer?
NM_138701.3:c.227del NP_619646.1:p.Gly76AlafsTer?
NM_138701.4:c.227del MANE Select NP_619646.1:p.Gly76AlafsTer?
Search 100 bp 5'
Search 100 bp 3'