Canonical Allele Identifier: CA60471514

Gene: STK39

Linked Data

• dbSNP Id: rs11393597
• gnomAD v2: 2-169041157-C-CT
• gnomAD v3: 2-168184647-C-CT
• gnomAD v4: 2-168184647-C-CT
• MyVariant Identifiers: chr2:g.169041157_169041158insT (hg19) ; chr2:g.168184647_168184648insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.168184647_168184648insT , CM000664.2:g.168184647_168184648insT	GRCh38
NC_000002.11:g.169041157_169041158insT , CM000664.1:g.169041157_169041158insT	GRCh37
NC_000002.10:g.168749403_168749404insT	NCBI36
NG_052783.1:g.67948_67949insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000697205.1:c.209-2558_209-2557insA	ENSP00000513185.1:n.209-2558_209-2557insA...
ENST00000355999.5:c.209-2558_209-2557insA MANE Select	ENSP00000348278.4:n.209-2558_209-2557insA...
ENST00000355999.4:c.209-2558_209-2557insA	ENSP00000348278.4:n.209-2558_209-2557insA...
NM_013233.2:c.209-2558_209-2557insA	NP_037365.2:n.209-2558_209-2557insA
XM_005246465.2:c.209-2558_209-2557insA	XP_005246522.1:n.209-2558_209-2557insA
XM_011510966.1:c.209-2558_209-2557insA	XP_011509268.1:n.209-2558_209-2557insA
XM_011510967.1:c.209-2558_209-2557insA	XP_011509269.1:n.209-2558_209-2557insA
XM_011510968.1:c.209-2558_209-2557insA	XP_011509270.1:n.209-2558_209-2557insA
XM_017003813.2:c.209-2558_209-2557insA	XP_016859302.1:n.209-2558_209-2557insA
XM_017003814.2:c.209-2558_209-2557insA	XP_016859303.1:n.209-2558_209-2557insA
XM_017003815.2:c.-98-2558_-98-2557insA	XP_016859304.1:n.-98-2558_-98-2557insA
XM_017003816.2:c.209-2558_209-2557insA	XP_016859305.1:n.209-2558_209-2557insA
NM_013233.3:c.209-2558_209-2557insA MANE Select	NP_037365.2:n.209-2558_209-2557insA