Canonical Allele Identifier: CA1305871147
Gene: STK39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168184821T= , CM000664.2:g.168184821T= GRCh38
NC_000002.11:g.169041331T= , CM000664.1:g.169041331T= GRCh37
NC_000002.10:g.168749577T= NCBI36
NG_052783.1:g.67775A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355999.5:c.209-2731A= MANE Select ENSP00000348278.4:n.209-2731A=
ENST00000355999.4:c.209-2731A= ENSP00000348278.4:n.209-2731A=
NM_013233.2:c.209-2731A= NP_037365.2:n.209-2731A=
XM_005246465.2:c.209-2731A= XP_005246522.1:n.209-2731A=
XM_011510966.1:c.209-2731A= XP_011509268.1:n.209-2731A=
XM_011510967.1:c.209-2731A= XP_011509269.1:n.209-2731A=
XM_011510968.1:c.209-2731A= XP_011509270.1:n.209-2731A=
XM_017003813.2:c.209-2731A= XP_016859302.1:n.209-2731A=
XM_017003814.2:c.209-2731A= XP_016859303.1:n.209-2731A=
XM_017003815.2:c.-98-2731A= XP_016859304.1:n.-98-2731A=
XM_017003816.2:c.209-2731A= XP_016859305.1:n.209-2731A=
NM_013233.3:c.209-2731A= MANE Select NP_037365.2:n.209-2731A=