Canonical Allele Identifier: CA1305871142
Gene: STK39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168184808C= , CM000664.2:g.168184808C= GRCh38
NC_000002.11:g.169041318C= , CM000664.1:g.169041318C= GRCh37
NC_000002.10:g.168749564C= NCBI36
NG_052783.1:g.67788G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355999.5:c.209-2718G= MANE Select ENSP00000348278.4:n.209-2718G=
ENST00000355999.4:c.209-2718G= ENSP00000348278.4:n.209-2718G=
NM_013233.2:c.209-2718G= NP_037365.2:n.209-2718G=
XM_005246465.2:c.209-2718G= XP_005246522.1:n.209-2718G=
XM_011510966.1:c.209-2718G= XP_011509268.1:n.209-2718G=
XM_011510967.1:c.209-2718G= XP_011509269.1:n.209-2718G=
XM_011510968.1:c.209-2718G= XP_011509270.1:n.209-2718G=
XM_017003813.2:c.209-2718G= XP_016859302.1:n.209-2718G=
XM_017003814.2:c.209-2718G= XP_016859303.1:n.209-2718G=
XM_017003815.2:c.-98-2718G= XP_016859304.1:n.-98-2718G=
XM_017003816.2:c.209-2718G= XP_016859305.1:n.209-2718G=
NM_013233.3:c.209-2718G= MANE Select NP_037365.2:n.209-2718G=