Canonical Allele Identifier: CA132154908

Gene: STK10

Linked Data

• dbSNP Id: rs1053622956
• gnomAD v2: 5-171559395-GA-G
• gnomAD v3: 5-172132391-GA-G
• gnomAD v4: 5-172132391-GA-G
• MyVariant Identifiers: chr5:g.171559396del (hg19) ; chr5:g.172132392del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.172132393del , CM000667.2:g.172132393del	GRCh38
NC_000005.9:g.171559397del , CM000667.1:g.171559397del	GRCh37
NC_000005.8:g.171492002del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000176763.10:c.322-4971del MANE Select	ENSP00000176763.5:n.322-4971del
ENST00000176763.9:c.322-4971del	ENSP00000176763.5:n.322-4971del
ENST00000519710.1:n.103-4971del
NM_005990.3:c.322-4971del	NP_005981.3:n.322-4971del
XM_011534641.1:c.322-4971del	XP_011532943.1:n.322-4971del
XM_011534643.1:c.322-4971del	XP_011532945.1:n.322-4971del
XM_011534644.1:c.322-4971del	XP_011532946.1:n.322-4971del
XM_017009788.1:c.-3-4971del	XP_016865277.1:n.-3-4971del
NM_005990.4:c.322-4971del MANE Select	NP_005981.3:n.322-4971del