Canonical Allele Identifier: CA1305871158

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168184845A= , CM000664.2:g.168184845A=	GRCh38
NC_000002.11:g.169041355A= , CM000664.1:g.169041355A=	GRCh37
NC_000002.10:g.168749601A=	NCBI36
NG_052783.1:g.67751T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.209-2755T=	ENSP00000513185.1:n.209-2755T=
ENST00000355999.5:c.209-2755T= MANE Select	ENSP00000348278.4:n.209-2755T=
ENST00000355999.4:c.209-2755T=	ENSP00000348278.4:n.209-2755T=
NM_013233.2:c.209-2755T=	NP_037365.2:n.209-2755T=
XM_005246465.2:c.209-2755T=	XP_005246522.1:n.209-2755T=
XM_011510966.1:c.209-2755T=	XP_011509268.1:n.209-2755T=
XM_011510967.1:c.209-2755T=	XP_011509269.1:n.209-2755T=
XM_011510968.1:c.209-2755T=	XP_011509270.1:n.209-2755T=
XM_017003813.2:c.209-2755T=	XP_016859302.1:n.209-2755T=
XM_017003814.2:c.209-2755T=	XP_016859303.1:n.209-2755T=
XM_017003815.2:c.-98-2755T=	XP_016859304.1:n.-98-2755T=
XM_017003816.2:c.209-2755T=	XP_016859305.1:n.209-2755T=
NM_013233.3:c.209-2755T= MANE Select	NP_037365.2:n.209-2755T=