Canonical Allele Identifier: CA2606367204

Gene: STK39

Linked Data

• gnomAD v3: 2-167954888-CAT-C
• gnomAD v4: 2-167954888-CAT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.167954892_167954893del , CM000664.2:g.167954892_167954893del	GRCh38
NC_000002.11:g.168811402_168811403del , CM000664.1:g.168811402_168811403del	GRCh37
NC_000002.10:g.168519648_168519649del	NCBI36
NG_052783.1:g.297706_297707del

Transcript Alleles

HGVS	Amino-acid change
ENST00000697205.1:c.2181_2182del	ENSP00000513185.1:n.2181_2182del
ENST00000355999.5:c.*606_*607del MANE Select	ENSP00000348278.4:n.*606_*607del
ENST00000355999.4:c.*606_*607del	ENSP00000348278.4:n.*606_*607del
ENST00000487143.5:n.1344_1345del
NM_013233.2:c.*606_*607del	NP_037365.2:n.*606_*607del
XM_005246465.2:c.*606_*607del	XP_005246522.1:n.*606_*607del
XM_011510966.1:c.*606_*607del	XP_011509268.1:n.*606_*607del
XM_011510967.1:c.*606_*607del	XP_011509269.1:n.*606_*607del
NM_013233.3:c.*606_*607del MANE Select	NP_037365.2:n.*606_*607del