Canonical Allele Identifier: CA2753071199
Gene: STK39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954845A>T , CM000664.2:g.167954845A>T GRCh38
NC_000002.11:g.168811355A>T , CM000664.1:g.168811355A>T GRCh37
NC_000002.10:g.168519601A>T NCBI36
NG_052783.1:g.297751T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.2226T>A ENSP00000513185.1:n.2226T>A
ENST00000355999.5:c.*651T>A MANE Select ENSP00000348278.4:n.*651T>A
ENST00000355999.4:c.*651T>A ENSP00000348278.4:n.*651T>A
ENST00000487143.5:n.1389T>A
NM_013233.2:c.*651T>A NP_037365.2:n.*651T>A
XM_005246465.2:c.*651T>A XP_005246522.1:n.*651T>A
XM_011510966.1:c.*651T>A XP_011509268.1:n.*651T>A
XM_011510967.1:c.*651T>A XP_011509269.1:n.*651T>A
NM_013233.3:c.*651T>A MANE Select NP_037365.2:n.*651T>A
Search 100 bp 5'
Search 100 bp 3'