Canonical Allele Identifier: CA304016603

Gene: STK11

Linked Data

• dbSNP Id: rs1048312061
• gnomAD v3: 19-1206849-CAAGG-C
• gnomAD v4: 19-1206849-CAAGG-C
• MyVariant Identifiers: chr19:g.1206849_1206852del (hg19) ; chr19:g.1206850_1206853del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206855_1206858del , CM000681.2:g.1206855_1206858del	GRCh38
NC_000019.9:g.1206854_1206857del , CM000681.1:g.1206854_1206857del	GRCh37
NC_000019.8:g.1157854_1157857del	NCBI36
NG_007460.2:g.22449_22452del , LRG_319:g.22449_22452del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.-59_-56del	ENSP00000490268.2:n.-59_-56del
ENST00000585748.3:c.-82-11562_-82-11559del	ENSP00000477641.2:n.-82-11562_-82-11559de...
ENST00000326873.12:c.-59_-56del MANE Select	ENSP00000324856.6:n.-59_-56del
ENST00000652231.1:c.-59_-56del	ENSP00000498804.1:n.-59_-56del
ENST00000326873.11:c.-59_-56del	ENSP00000324856.6:n.-59_-56del
ENST00000585748.2:c.-82-11562_-82-11559del	ENSP00000477641.1:n.-82-11562_-82-11559de...
ENST00000586243.5:c.-59_-56del	ENSP00000467240.2:n.-59_-56del
ENST00000589152.5:n.32_35del
ENST00000593219.5:c.-59_-56del	ENSP00000466610.1:n.-59_-56del
NM_000455.4:c.-59_-56del , LRG_319t1:c.-59_-56del	NP_000446.1:n.-59_-56del
XM_005259617.1:c.-59_-56del	XP_005259674.1:n.-59_-56del
XM_005259618.3:c.-59_-56del	XP_005259675.1:n.-59_-56del
XM_011528209.1:c.-412_-409del	XP_011526511.1:n.-412_-409del
XR_936204.1:n.567_570del
XM_005259617.3:c.-59_-56del	XP_005259674.1:n.-59_-56del
XM_011528209.2:c.-412_-409del	XP_011526511.1:n.-412_-409del
XR_001753738.2:n.567_570del
XR_001753739.1:n.567_570del
XR_001753740.2:n.567_570del
NM_000455.5:c.-59_-56del MANE Select	NP_000446.1:n.-59_-56del