Canonical Allele Identifier: CA2769429145

Gene: STK10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132482G>C , CM000667.2:g.172132482G>C	GRCh38
NC_000005.9:g.171559486G>C , CM000667.1:g.171559486G>C	GRCh37
NC_000005.8:g.171492091G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176763.10:c.322-5061C>G MANE Select	ENSP00000176763.5:n.322-5061C>G
ENST00000176763.9:c.322-5061C>G	ENSP00000176763.5:n.322-5061C>G
ENST00000519710.1:n.103-5061C>G
NM_005990.3:c.322-5061C>G	NP_005981.3:n.322-5061C>G
XM_011534641.1:c.322-5061C>G	XP_011532943.1:n.322-5061C>G
XM_011534643.1:c.322-5061C>G	XP_011532945.1:n.322-5061C>G
XM_011534644.1:c.322-5061C>G	XP_011532946.1:n.322-5061C>G
XM_017009788.1:c.-3-5061C>G	XP_016865277.1:n.-3-5061C>G
NM_005990.4:c.322-5061C>G MANE Select	NP_005981.3:n.322-5061C>G