Canonical Allele Identifier: CA1305769359

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954789_167954790delinsCA , CM000664.2:g.167954789_167954790delinsCA	GRCh38
NC_000002.11:g.168811299_168811300delinsCA , CM000664.1:g.168811299_168811300delinsCA	GRCh37
NC_000002.10:g.168519545_168519546delinsCA	NCBI36
NG_052783.1:g.297806_297807delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.2281_2282delinsTG	ENSP00000513185.1:n.2281_2282delinsTG
ENST00000355999.5:c.*706_*707delinsTG MANE Select	ENSP00000348278.4:n.*706_*707delinsTG
ENST00000355999.4:c.*706_*707delinsTG	ENSP00000348278.4:n.*706_*707delinsTG
ENST00000487143.5:n.1444_1445delinsTG
NM_013233.2:c.*706_*707delinsTG	NP_037365.2:n.*706_*707delinsTG
XM_005246465.2:c.*706_*707delinsTG	XP_005246522.1:n.*706_*707delinsTG
XM_011510966.1:c.*706_*707delinsTG	XP_011509268.1:n.*706_*707delinsTG
XM_011510967.1:c.*706_*707delinsTG	XP_011509269.1:n.*706_*707delinsTG
NM_013233.3:c.*706_*707delinsTG MANE Select	NP_037365.2:n.*706_*707delinsTG