Canonical Allele Identifier: CA2661783603
Gene: STK39 HGNC NCBI

Linked Data

gnomAD v4: 2-167954770-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954770G>T , CM000664.2:g.167954770G>T GRCh38
NC_000002.11:g.168811280G>T , CM000664.1:g.168811280G>T GRCh37
NC_000002.10:g.168519526G>T NCBI36
NG_052783.1:g.297826C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697205.1:c.2301C>A ENSP00000513185.1:n.2301C>A
ENST00000355999.5:c.*726C>A MANE Select ENSP00000348278.4:n.*726C>A
ENST00000355999.4:c.*726C>A ENSP00000348278.4:n.*726C>A
ENST00000487143.5:n.1464C>A
NM_013233.2:c.*726C>A NP_037365.2:n.*726C>A
XM_005246465.2:c.*726C>A XP_005246522.1:n.*726C>A
XM_011510966.1:c.*726C>A XP_011509268.1:n.*726C>A
XM_011510967.1:c.*726C>A XP_011509269.1:n.*726C>A
NM_013233.3:c.*726C>A MANE Select NP_037365.2:n.*726C>A
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