Canonical Allele Identifier: CA1601146882

Gene: STK10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132361_172132370delinsCTAGGGGCTT , CM000667.2:g.172132361_172132370delinsCTAGGGGCTT	GRCh38
NC_000005.9:g.171559365_171559374delinsCTAGGGGCTT , CM000667.1:g.171559365_171559374delinsCTAGGGGCTT	GRCh37
NC_000005.8:g.171491970_171491979delinsCTAGGGGCTT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176763.10:c.322-4949_322-4940delinsAAGCCCCTAG MANE Select	ENSP00000176763.5:n.322-4949_322-4940delinsAAGCCCCTAG
ENST00000176763.9:c.322-4949_322-4940delinsAAGCCCCTAG	ENSP00000176763.5:n.322-4949_322-4940delinsAAGCCCCTAG
ENST00000519710.1:n.103-4949_103-4940delinsAAGCCCCTAG
NM_005990.3:c.322-4949_322-4940delinsAAGCCCCTAG	NP_005981.3:n.322-4949_322-4940delinsAAGCCCCTAG
XM_011534641.1:c.322-4949_322-4940delinsAAGCCCCTAG	XP_011532943.1:n.322-4949_322-4940delinsAAGCCCCTAG
XM_011534643.1:c.322-4949_322-4940delinsAAGCCCCTAG	XP_011532945.1:n.322-4949_322-4940delinsAAGCCCCTAG
XM_011534644.1:c.322-4949_322-4940delinsAAGCCCCTAG	XP_011532946.1:n.322-4949_322-4940delinsAAGCCCCTAG
XM_017009788.1:c.-3-4949_-3-4940delinsAAGCCCCTAG	XP_016865277.1:n.-3-4949_-3-4940delinsAAGCCCCTAG
NM_005990.4:c.322-4949_322-4940delinsAAGCCCCTAG MANE Select	NP_005981.3:n.322-4949_322-4940delinsAAGCCCCTAG