Canonical Allele Identifier: CA1305769388

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954894A= , CM000664.2:g.167954894A=	GRCh38
NC_000002.11:g.168811404A= , CM000664.1:g.168811404A=	GRCh37
NC_000002.10:g.168519650A=	NCBI36
NG_052783.1:g.297702T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697205.1:c.2177T=	ENSP00000513185.1:n.2177T=
ENST00000355999.5:c.*602T= MANE Select	ENSP00000348278.4:n.*602T=
ENST00000355999.4:c.*602T=	ENSP00000348278.4:n.*602T=
ENST00000487143.5:n.1340T=
NM_013233.2:c.*602T=	NP_037365.2:n.*602T=
XM_005246465.2:c.*602T=	XP_005246522.1:n.*602T=
XM_011510966.1:c.*602T=	XP_011509268.1:n.*602T=
XM_011510967.1:c.*602T=	XP_011509269.1:n.*602T=
NM_013233.3:c.*602T= MANE Select	NP_037365.2:n.*602T=