Canonical Allele Identifier: CA2971617233

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168184941_168184942insT , CM000664.2:g.168184941_168184942insT	GRCh38
NC_000002.11:g.169041451_169041452insT , CM000664.1:g.169041451_169041452insT	GRCh37
NC_000002.10:g.168749697_168749698insT	NCBI36
NG_052783.1:g.67654_67655insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.209-2852_209-2851insA	ENSP00000513185.1:n.209-2852_209-2851insA
ENST00000355999.5:c.209-2852_209-2851insA MANE Select	ENSP00000348278.4:n.209-2852_209-2851insA
ENST00000355999.4:c.209-2852_209-2851insA	ENSP00000348278.4:n.209-2852_209-2851insA
NM_013233.2:c.209-2852_209-2851insA	NP_037365.2:n.209-2852_209-2851insA
XM_005246465.2:c.209-2852_209-2851insA	XP_005246522.1:n.209-2852_209-2851insA
XM_011510966.1:c.209-2852_209-2851insA	XP_011509268.1:n.209-2852_209-2851insA
XM_011510967.1:c.209-2852_209-2851insA	XP_011509269.1:n.209-2852_209-2851insA
XM_011510968.1:c.209-2852_209-2851insA	XP_011509270.1:n.209-2852_209-2851insA
XM_017003813.2:c.209-2852_209-2851insA	XP_016859302.1:n.209-2852_209-2851insA
XM_017003814.2:c.209-2852_209-2851insA	XP_016859303.1:n.209-2852_209-2851insA
XM_017003815.2:c.-98-2852_-98-2851insA	XP_016859304.1:n.-98-2852_-98-2851insA
XM_017003816.2:c.209-2852_209-2851insA	XP_016859305.1:n.209-2852_209-2851insA
NM_013233.3:c.209-2852_209-2851insA MANE Select	NP_037365.2:n.209-2852_209-2851insA