Canonical Allele Identifier: CA631299707

Gene: STK11

Linked Data

• dbSNP Id: rs1217183530
• gnomAD v2: 19-1206732-AC-A
• gnomAD v3: 19-1206733-AC-A
• gnomAD v4: 19-1206733-AC-A
• MyVariant Identifiers: chr19:g.1206733del (hg19) ; chr19:g.1206734del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206734del , CM000681.2:g.1206734del	GRCh38
NC_000019.9:g.1206733del , CM000681.1:g.1206733del	GRCh37
NC_000019.8:g.1157733del	NCBI36
NG_007460.2:g.22328del , LRG_319:g.22328del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-180del	ENSP00000490268.2:n.-180del
ENST00000585748.3:c.-82-11683del	ENSP00000477641.2:n.-82-11683del
ENST00000326873.12:c.-180del MANE Select	ENSP00000324856.6:n.-180del
ENST00000652231.1:c.-180del	ENSP00000498804.1:n.-180del
ENST00000326873.11:c.-180del	ENSP00000324856.6:n.-180del
ENST00000585748.2:c.-82-11683del	ENSP00000477641.1:n.-82-11683del
ENST00000586243.5:c.-180del	ENSP00000467240.2:n.-180del
NM_000455.4:c.-180del , LRG_319t1:c.-180del	NP_000446.1:n.-180del
XM_005259617.1:c.-180del	XP_005259674.1:n.-180del
XM_005259618.3:c.-180del	XP_005259675.1:n.-180del
XM_011528209.1:c.-533del	XP_011526511.1:n.-533del
XR_936204.1:n.446del
XM_005259617.3:c.-180del	XP_005259674.1:n.-180del
XM_011528209.2:c.-533del	XP_011526511.1:n.-533del
XR_001753738.2:n.446del
XR_001753739.1:n.446del
XR_001753740.2:n.446del
NM_000455.5:c.-180del MANE Select	NP_000446.1:n.-180del