Canonical Allele Identifier: CA1305769390

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954900_167954901delinsAC , CM000664.2:g.167954900_167954901delinsAC	GRCh38
NC_000002.11:g.168811410_168811411delinsAC , CM000664.1:g.168811410_168811411delinsAC	GRCh37
NC_000002.10:g.168519656_168519657delinsAC	NCBI36
NG_052783.1:g.297695_297696delinsGT

Transcript Alleles

HGVS	Amino-acid change
ENST00000697205.1:c.2170_2171delinsGT	ENSP00000513185.1:n.2170_2171delinsGT
ENST00000355999.5:c.*595_*596delinsGT MANE Select	ENSP00000348278.4:n.*595_*596delinsGT
ENST00000355999.4:c.*595_*596delinsGT	ENSP00000348278.4:n.*595_*596delinsGT
ENST00000487143.5:n.1333_1334delinsGT
NM_013233.2:c.*595_*596delinsGT	NP_037365.2:n.*595_*596delinsGT
XM_005246465.2:c.*595_*596delinsGT	XP_005246522.1:n.*595_*596delinsGT
XM_011510966.1:c.*595_*596delinsGT	XP_011509268.1:n.*595_*596delinsGT
XM_011510967.1:c.*595_*596delinsGT	XP_011509269.1:n.*595_*596delinsGT
NM_013233.3:c.*595_*596delinsGT MANE Select	NP_037365.2:n.*595_*596delinsGT