Canonical Allele Identifier: CA1305769383

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954870G= , CM000664.2:g.167954870G=	GRCh38
NC_000002.11:g.168811380G= , CM000664.1:g.168811380G=	GRCh37
NC_000002.10:g.168519626G=	NCBI36
NG_052783.1:g.297726C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000697205.1:c.2201C=	ENSP00000513185.1:n.2201C=
ENST00000355999.5:c.*626C= MANE Select	ENSP00000348278.4:n.*626C=
ENST00000355999.4:c.*626C=	ENSP00000348278.4:n.*626C=
ENST00000487143.5:n.1364C=
NM_013233.2:c.*626C=	NP_037365.2:n.*626C=
XM_005246465.2:c.*626C=	XP_005246522.1:n.*626C=
XM_011510966.1:c.*626C=	XP_011509268.1:n.*626C=
XM_011510967.1:c.*626C=	XP_011509269.1:n.*626C=
NM_013233.3:c.*626C= MANE Select	NP_037365.2:n.*626C=