Canonical Allele Identifier: CA1084423007

Gene: STK10

Linked Data

• dbSNP Id: rs1769773611
• gnomAD v3: 5-172132361-CTAGGGGCTT-C
• gnomAD v4: 5-172132361-CTAGGGGCTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132365_172132373del , CM000667.2:g.172132365_172132373del	GRCh38
NC_000005.9:g.171559369_171559377del , CM000667.1:g.171559369_171559377del	GRCh37
NC_000005.8:g.171491974_171491982del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176763.10:c.322-4949_322-4941del MANE Select	ENSP00000176763.5:n.322-4949_322-4941del
ENST00000176763.9:c.322-4949_322-4941del	ENSP00000176763.5:n.322-4949_322-4941del
ENST00000519710.1:n.103-4949_103-4941del
NM_005990.3:c.322-4949_322-4941del	NP_005981.3:n.322-4949_322-4941del
XM_011534641.1:c.322-4949_322-4941del	XP_011532943.1:n.322-4949_322-4941del
XM_011534643.1:c.322-4949_322-4941del	XP_011532945.1:n.322-4949_322-4941del
XM_011534644.1:c.322-4949_322-4941del	XP_011532946.1:n.322-4949_322-4941del
XM_017009788.1:c.-3-4949_-3-4941del	XP_016865277.1:n.-3-4949_-3-4941del
NM_005990.4:c.322-4949_322-4941del MANE Select	NP_005981.3:n.322-4949_322-4941del