Canonical Allele Identifier: CA1084423015
Gene: STK10 HGNC NCBI

Linked Data

dbSNP Id: rs201600763

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.172132382del , CM000667.2:g.172132382del GRCh38
NC_000005.9:g.171559386del , CM000667.1:g.171559386del GRCh37
NC_000005.8:g.171491991del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000176763.10:c.322-4953del MANE Select ENSP00000176763.5:n.322-4953del
ENST00000176763.9:c.322-4953del ENSP00000176763.5:n.322-4953del
ENST00000519710.1:n.103-4953del
NM_005990.3:c.322-4953del NP_005981.3:n.322-4953del
XM_011534641.1:c.322-4953del XP_011532943.1:n.322-4953del
XM_011534643.1:c.322-4953del XP_011532945.1:n.322-4953del
XM_011534644.1:c.322-4953del XP_011532946.1:n.322-4953del
XM_017009788.1:c.-3-4953del XP_016865277.1:n.-3-4953del
NM_005990.4:c.322-4953del MANE Select NP_005981.3:n.322-4953del