Canonical Allele Identifier: CA2661783606
Gene: STK39 HGNC NCBI

Linked Data

gnomAD v4: 2-167954791-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954791A>G , CM000664.2:g.167954791A>G GRCh38
NC_000002.11:g.168811301A>G , CM000664.1:g.168811301A>G GRCh37
NC_000002.10:g.168519547A>G NCBI36
NG_052783.1:g.297805T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697205.1:c.2280T>C ENSP00000513185.1:n.2280T>C
ENST00000355999.5:c.*705T>C MANE Select ENSP00000348278.4:n.*705T>C
ENST00000355999.4:c.*705T>C ENSP00000348278.4:n.*705T>C
ENST00000487143.5:n.1443T>C
NM_013233.2:c.*705T>C NP_037365.2:n.*705T>C
XM_005246465.2:c.*705T>C XP_005246522.1:n.*705T>C
XM_011510966.1:c.*705T>C XP_011509268.1:n.*705T>C
XM_011510967.1:c.*705T>C XP_011509269.1:n.*705T>C
NM_013233.3:c.*705T>C MANE Select NP_037365.2:n.*705T>C
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