Canonical Allele Identifier: CA1305871131
Gene: STK39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168184781G= , CM000664.2:g.168184781G= GRCh38
NC_000002.11:g.169041291G= , CM000664.1:g.169041291G= GRCh37
NC_000002.10:g.168749537G= NCBI36
NG_052783.1:g.67815C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355999.5:c.209-2691C= MANE Select ENSP00000348278.4:n.209-2691C=
ENST00000355999.4:c.209-2691C= ENSP00000348278.4:n.209-2691C=
NM_013233.2:c.209-2691C= NP_037365.2:n.209-2691C=
XM_005246465.2:c.209-2691C= XP_005246522.1:n.209-2691C=
XM_011510966.1:c.209-2691C= XP_011509268.1:n.209-2691C=
XM_011510967.1:c.209-2691C= XP_011509269.1:n.209-2691C=
XM_011510968.1:c.209-2691C= XP_011509270.1:n.209-2691C=
XM_017003813.2:c.209-2691C= XP_016859302.1:n.209-2691C=
XM_017003814.2:c.209-2691C= XP_016859303.1:n.209-2691C=
XM_017003815.2:c.-98-2691C= XP_016859304.1:n.-98-2691C=
XM_017003816.2:c.209-2691C= XP_016859305.1:n.209-2691C=
NM_013233.3:c.209-2691C= MANE Select NP_037365.2:n.209-2691C=