Canonical Allele Identifier: CA1305769391
Gene: STK39 HGNC NCBI

Linked Data

dbSNP Id: rs1691722908

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954903del , CM000664.2:g.167954903del GRCh38
NC_000002.11:g.168811413del , CM000664.1:g.168811413del GRCh37
NC_000002.10:g.168519659del NCBI36
NG_052783.1:g.297695del

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.2170del ENSP00000513185.1:n.2170del
ENST00000355999.5:c.*595del MANE Select ENSP00000348278.4:n.*595del
ENST00000355999.4:c.*595del ENSP00000348278.4:n.*595del
ENST00000487143.5:n.1333del
NM_013233.2:c.*595del NP_037365.2:n.*595del
XM_005246465.2:c.*595del XP_005246522.1:n.*595del
XM_011510966.1:c.*595del XP_011509268.1:n.*595del
XM_011510967.1:c.*595del XP_011509269.1:n.*595del
NM_013233.3:c.*595del MANE Select NP_037365.2:n.*595del