Canonical Allele Identifier: CA2753071200
Gene: STK39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954905_167954910dup , CM000664.2:g.167954905_167954910dup GRCh38
NC_000002.11:g.168811415_168811420dup , CM000664.1:g.168811415_168811420dup GRCh37
NC_000002.10:g.168519661_168519666dup NCBI36
NG_052783.1:g.297687_297692dup

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.2162_2167dup ENSP00000513185.1:n.2162_2167dup
ENST00000355999.5:c.*587_*592dup MANE Select ENSP00000348278.4:n.*587_*592dup
ENST00000355999.4:c.*587_*592dup ENSP00000348278.4:n.*587_*592dup
ENST00000487143.5:n.1325_1330dup
NM_013233.2:c.*587_*592dup NP_037365.2:n.*587_*592dup
XM_005246465.2:c.*587_*592dup XP_005246522.1:n.*587_*592dup
XM_011510966.1:c.*587_*592dup XP_011509268.1:n.*587_*592dup
XM_011510967.1:c.*587_*592dup XP_011509269.1:n.*587_*592dup
NM_013233.3:c.*587_*592dup MANE Select NP_037365.2:n.*587_*592dup