Canonical Allele Identifier: CA60471500

Gene: STK39

Linked Data

• dbSNP Id: rs67284354
• gnomAD v2: 2-169041038-AACCC-A
• gnomAD v3: 2-168184528-AACCC-A
• gnomAD v4: 2-168184528-AACCC-A
• MyVariant Identifiers: chr2:g.169041039_169041042del (hg19) ; chr2:g.168184529_168184532del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168184533_168184536del , CM000664.2:g.168184533_168184536del	GRCh38
NC_000002.11:g.169041043_169041046del , CM000664.1:g.169041043_169041046del	GRCh37
NC_000002.10:g.168749289_168749292del	NCBI36
NG_052783.1:g.68064_68067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697205.1:c.209-2442_209-2439del	ENSP00000513185.1:n.209-2442_209-2439del
ENST00000355999.5:c.209-2442_209-2439del MANE Select	ENSP00000348278.4:n.209-2442_209-2439del
ENST00000355999.4:c.209-2442_209-2439del	ENSP00000348278.4:n.209-2442_209-2439del
NM_013233.2:c.209-2442_209-2439del	NP_037365.2:n.209-2442_209-2439del
XM_005246465.2:c.209-2442_209-2439del	XP_005246522.1:n.209-2442_209-2439del
XM_011510966.1:c.209-2442_209-2439del	XP_011509268.1:n.209-2442_209-2439del
XM_011510967.1:c.209-2442_209-2439del	XP_011509269.1:n.209-2442_209-2439del
XM_011510968.1:c.209-2442_209-2439del	XP_011509270.1:n.209-2442_209-2439del
XM_017003813.2:c.209-2442_209-2439del	XP_016859302.1:n.209-2442_209-2439del
XM_017003814.2:c.209-2442_209-2439del	XP_016859303.1:n.209-2442_209-2439del
XM_017003815.2:c.-98-2442_-98-2439del	XP_016859304.1:n.-98-2442_-98-2439del
XM_017003816.2:c.209-2442_209-2439del	XP_016859305.1:n.209-2442_209-2439del
NM_013233.3:c.209-2442_209-2439del MANE Select	NP_037365.2:n.209-2442_209-2439del