Canonical Allele Identifier: CA2661783617
Gene: STK39 HGNC NCBI

Linked Data

gnomAD v4: 2-167954849-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954849A>C , CM000664.2:g.167954849A>C GRCh38
NC_000002.11:g.168811359A>C , CM000664.1:g.168811359A>C GRCh37
NC_000002.10:g.168519605A>C NCBI36
NG_052783.1:g.297747T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.2222T>G ENSP00000513185.1:n.2222T>G
ENST00000355999.5:c.*647T>G MANE Select ENSP00000348278.4:n.*647T>G
ENST00000355999.4:c.*647T>G ENSP00000348278.4:n.*647T>G
ENST00000487143.5:n.1385T>G
NM_013233.2:c.*647T>G NP_037365.2:n.*647T>G
XM_005246465.2:c.*647T>G XP_005246522.1:n.*647T>G
XM_011510966.1:c.*647T>G XP_011509268.1:n.*647T>G
XM_011510967.1:c.*647T>G XP_011509269.1:n.*647T>G
NM_013233.3:c.*647T>G MANE Select NP_037365.2:n.*647T>G
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