Canonical Allele Identifier: CA1305769360

Gene: STK39

Linked Data

• dbSNP Id: rs1691720749

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954792del , CM000664.2:g.167954792del	GRCh38
NC_000002.11:g.168811302del , CM000664.1:g.168811302del	GRCh37
NC_000002.10:g.168519548del	NCBI36
NG_052783.1:g.297806del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.2281del	ENSP00000513185.1:n.2281del
ENST00000355999.5:c.*706del MANE Select	ENSP00000348278.4:n.*706del
ENST00000355999.4:c.*706del	ENSP00000348278.4:n.*706del
ENST00000487143.5:n.1444del
NM_013233.2:c.*706del	NP_037365.2:n.*706del
XM_005246465.2:c.*706del	XP_005246522.1:n.*706del
XM_011510966.1:c.*706del	XP_011509268.1:n.*706del
XM_011510967.1:c.*706del	XP_011509269.1:n.*706del
NM_013233.3:c.*706del MANE Select	NP_037365.2:n.*706del