Canonical Allele Identifier: CA1305769397

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954904T= , CM000664.2:g.167954904T=	GRCh38
NC_000002.11:g.168811414T= , CM000664.1:g.168811414T=	GRCh37
NC_000002.10:g.168519660T=	NCBI36
NG_052783.1:g.297692A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697205.1:c.2167A=	ENSP00000513185.1:n.2167A=
ENST00000355999.5:c.*592A= MANE Select	ENSP00000348278.4:n.*592A=
ENST00000355999.4:c.*592A=	ENSP00000348278.4:n.*592A=
ENST00000487143.5:n.1330A=
NM_013233.2:c.*592A=	NP_037365.2:n.*592A=
XM_005246465.2:c.*592A=	XP_005246522.1:n.*592A=
XM_011510966.1:c.*592A=	XP_011509268.1:n.*592A=
XM_011510967.1:c.*592A=	XP_011509269.1:n.*592A=
NM_013233.3:c.*592A= MANE Select	NP_037365.2:n.*592A=