Canonical Allele Identifier: CA386365698
Gene: NUAK1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.106461197T>A (hg19) chr12:g.106067419T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.106067419T>A , CM000674.2:g.106067419T>A GRCh38
NC_000012.11:g.106461197T>A , CM000674.1:g.106461197T>A GRCh37
NC_000012.10:g.104985327T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000261402.7:c.1369A>T MANE Select ENSP00000261402.2:p.Lys457Ter
ENST00000261402.6:c.1369A>T ENSP00000261402.2:p.Lys457Ter
NM_014840.2:c.1369A>T NP_055655.1:p.Lys457Ter
NM_014840.3:c.1369A>T MANE Select NP_055655.1:p.Lys457Ter
Search 100 bp 5'
Search 100 bp 3'