Canonical Allele Identifier: CA2769429146

Gene: STK10

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132512A>G , CM000667.2:g.172132512A>G	GRCh38
NC_000005.9:g.171559516A>G , CM000667.1:g.171559516A>G	GRCh37
NC_000005.8:g.171492121A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000176763.10:c.322-5091T>C MANE Select	ENSP00000176763.5:n.322-5091T>C
ENST00000176763.9:c.322-5091T>C	ENSP00000176763.5:n.322-5091T>C
ENST00000519710.1:n.103-5091T>C
NM_005990.3:c.322-5091T>C	NP_005981.3:n.322-5091T>C
XM_011534641.1:c.322-5091T>C	XP_011532943.1:n.322-5091T>C
XM_011534643.1:c.322-5091T>C	XP_011532945.1:n.322-5091T>C
XM_011534644.1:c.322-5091T>C	XP_011532946.1:n.322-5091T>C
XM_017009788.1:c.-3-5091T>C	XP_016865277.1:n.-3-5091T>C
NM_005990.4:c.322-5091T>C MANE Select	NP_005981.3:n.322-5091T>C