Canonical Allele Identifier: CA537622609
Gene: STK39 HGNC NCBI

Linked Data

dbSNP Id: rs1197660394
gnomAD v2: 2-168811321-CA-C
gnomAD v3: 2-167954811-CA-C
gnomAD v4: 2-167954811-CA-C
MyVariant Identifiers: chr2:g.168811322del (hg19) chr2:g.167954812del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.167954815del , CM000664.2:g.167954815del GRCh38
NC_000002.11:g.168811325del , CM000664.1:g.168811325del GRCh37
NC_000002.10:g.168519571del NCBI36
NG_052783.1:g.297784del

Transcript Alleles

HGVS Amino-acid Change
ENST00000697205.1:c.2259del ENSP00000513185.1:n.2259del
ENST00000355999.5:c.*684del MANE Select ENSP00000348278.4:n.*684del
ENST00000355999.4:c.*684del ENSP00000348278.4:n.*684del
ENST00000487143.5:n.1422del
NM_013233.2:c.*684del NP_037365.2:n.*684del
XM_005246465.2:c.*684del XP_005246522.1:n.*684del
XM_011510966.1:c.*684del XP_011509268.1:n.*684del
XM_011510967.1:c.*684del XP_011509269.1:n.*684del
NM_013233.3:c.*684del MANE Select NP_037365.2:n.*684del
Search 100 bp 5'
Search 100 bp 3'