Canonical Allele Identifier: CA650875465

Gene: STK10

Linked Data

• COSMIC: COSN9420275 ; COSN15505517

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132565G>T , CM000667.2:g.172132565G>T	GRCh38
NC_000005.9:g.171559569G>T , CM000667.1:g.171559569G>T	GRCh37
NC_000005.8:g.171492174G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000176763.10:c.322-5144C>A MANE Select	ENSP00000176763.5:n.322-5144C>A
ENST00000176763.9:c.322-5144C>A	ENSP00000176763.5:n.322-5144C>A
ENST00000519710.1:n.103-5144C>A
NM_005990.3:c.322-5144C>A	NP_005981.3:n.322-5144C>A
XM_011534641.1:c.322-5144C>A	XP_011532943.1:n.322-5144C>A
XM_011534643.1:c.322-5144C>A	XP_011532945.1:n.322-5144C>A
XM_011534644.1:c.322-5144C>A	XP_011532946.1:n.322-5144C>A
XM_017009788.1:c.-3-5144C>A	XP_016865277.1:n.-3-5144C>A
NM_005990.4:c.322-5144C>A MANE Select	NP_005981.3:n.322-5144C>A