Canonical Allele Identifier: CA1601146950
Gene: STK10 HGNC NCBI

Linked Data

dbSNP Id: rs1769774606
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172132424_172132429del , CM000667.2:g.172132424_172132429del GRCh38
NC_000005.9:g.171559428_171559433del , CM000667.1:g.171559428_171559433del GRCh37
NC_000005.8:g.171492033_171492038del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000176763.10:c.322-5006_322-5001del MANE Select ENSP00000176763.5:n.322-5006_322-5001del
ENST00000176763.9:c.322-5006_322-5001del ENSP00000176763.5:n.322-5006_322-5001del
ENST00000519710.1:n.103-5006_103-5001del
NM_005990.3:c.322-5006_322-5001del NP_005981.3:n.322-5006_322-5001del
XM_011534641.1:c.322-5006_322-5001del XP_011532943.1:n.322-5006_322-5001del
XM_011534643.1:c.322-5006_322-5001del XP_011532945.1:n.322-5006_322-5001del
XM_011534644.1:c.322-5006_322-5001del XP_011532946.1:n.322-5006_322-5001del
XM_017009788.1:c.-3-5006_-3-5001del XP_016865277.1:n.-3-5006_-3-5001del
NM_005990.4:c.322-5006_322-5001del MANE Select NP_005981.3:n.322-5006_322-5001del
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