Canonical Allele Identifier: CA1305769393

Gene: STK39

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954903_167954904delinsCT , CM000664.2:g.167954903_167954904delinsCT	GRCh38
NC_000002.11:g.168811413_168811414delinsCT , CM000664.1:g.168811413_168811414delinsCT	GRCh37
NC_000002.10:g.168519659_168519660delinsCT	NCBI36
NG_052783.1:g.297692_297693delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000697205.1:c.2167_2168delinsAG	ENSP00000513185.1:n.2167_2168delinsAG
ENST00000355999.5:c.*592_*593delinsAG MANE Select	ENSP00000348278.4:n.*592_*593delinsAG
ENST00000355999.4:c.*592_*593delinsAG	ENSP00000348278.4:n.*592_*593delinsAG
ENST00000487143.5:n.1330_1331delinsAG
NM_013233.2:c.*592_*593delinsAG	NP_037365.2:n.*592_*593delinsAG
XM_005246465.2:c.*592_*593delinsAG	XP_005246522.1:n.*592_*593delinsAG
XM_011510966.1:c.*592_*593delinsAG	XP_011509268.1:n.*592_*593delinsAG
XM_011510967.1:c.*592_*593delinsAG	XP_011509269.1:n.*592_*593delinsAG
NM_013233.3:c.*592_*593delinsAG MANE Select	NP_037365.2:n.*592_*593delinsAG