Canonical Allele Identifier: CA11036638
Gene: STK39 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168159753C>T , CM000664.2:g.168159753C>T GRCh38
NC_000002.11:g.169016263C>T , CM000664.1:g.169016263C>T GRCh37
NC_000002.10:g.168724509C>T NCBI36
NG_052783.1:g.92843G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000697205.1:c.628+2034G>A ENSP00000513185.1:n.628+2034G>A
ENST00000355999.5:c.628+2034G>A MANE Select ENSP00000348278.4:n.628+2034G>A
ENST00000355999.4:c.628+2034G>A ENSP00000348278.4:n.628+2034G>A
NM_013233.2:c.628+2034G>A NP_037365.2:n.628+2034G>A
XM_005246465.2:c.628+2034G>A XP_005246522.1:n.628+2034G>A
XM_011510966.1:c.628+2034G>A XP_011509268.1:n.628+2034G>A
XM_011510967.1:c.628+2034G>A XP_011509269.1:n.628+2034G>A
XM_011510968.1:c.628+2034G>A XP_011509270.1:n.628+2034G>A
XM_017003813.2:c.628+2034G>A XP_016859302.1:n.628+2034G>A
XM_017003814.2:c.628+2034G>A XP_016859303.1:n.628+2034G>A
XM_017003815.2:c.322+2034G>A XP_016859304.1:n.322+2034G>A
XM_017003816.2:c.628+2034G>A XP_016859305.1:n.628+2034G>A
XM_017003817.2:c.136+2034G>A XP_016859306.1:n.136+2034G>A
NM_013233.3:c.628+2034G>A MANE Select NP_037365.2:n.628+2034G>A
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