Canonical Allele Identifier: CA2563207084
Gene: STK39 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.168184608_168184609insGTAA , CM000664.2:g.168184608_168184609insGTAA GRCh38
NC_000002.11:g.169041118_169041119insGTAA , CM000664.1:g.169041118_169041119insGTAA GRCh37
NC_000002.10:g.168749364_168749365insGTAA NCBI36
NG_052783.1:g.67988_67989insTACT

Transcript Alleles

HGVS Amino-acid change
ENST00000697205.1:c.209-2518_209-2517insTACT ENSP00000513185.1:n.209-2518_209-2517insT...
ENST00000355999.5:c.209-2518_209-2517insTACT MANE Select ENSP00000348278.4:n.209-2518_209-2517insT...
ENST00000355999.4:c.209-2518_209-2517insTACT ENSP00000348278.4:n.209-2518_209-2517insT...
NM_013233.2:c.209-2518_209-2517insTACT NP_037365.2:n.209-2518_209-2517insTACT
XM_005246465.2:c.209-2518_209-2517insTACT XP_005246522.1:n.209-2518_209-2517insTACT...
XM_011510966.1:c.209-2518_209-2517insTACT XP_011509268.1:n.209-2518_209-2517insTACT...
XM_011510967.1:c.209-2518_209-2517insTACT XP_011509269.1:n.209-2518_209-2517insTACT...
XM_011510968.1:c.209-2518_209-2517insTACT XP_011509270.1:n.209-2518_209-2517insTACT...
XM_017003813.2:c.209-2518_209-2517insTACT XP_016859302.1:n.209-2518_209-2517insTACT...
XM_017003814.2:c.209-2518_209-2517insTACT XP_016859303.1:n.209-2518_209-2517insTACT...
XM_017003815.2:c.-98-2518_-98-2517insTACT XP_016859304.1:n.-98-2518_-98-2517insTACT...
XM_017003816.2:c.209-2518_209-2517insTACT XP_016859305.1:n.209-2518_209-2517insTACT...
NM_013233.3:c.209-2518_209-2517insTACT MANE Select NP_037365.2:n.209-2518_209-2517insTACT