Canonical Allele Identifier: CA2317593487

Gene: STK11

Linked Data

• dbSNP Id: rs2080819357
• gnomAD v3: 19-1226207-GGTGCAA-G
• gnomAD v4: 19-1226207-GGTGCAA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226208_1226213del , CM000681.2:g.1226208_1226213del	GRCh38
NC_000019.9:g.1226207_1226212del , CM000681.1:g.1226207_1226212del	GRCh37
NC_000019.8:g.1177207_1177212del	NCBI36
NG_007460.2:g.41802_41807del , LRG_319:g.41802_41807del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2464_*2469del	ENSP00000490268.2:n.*2464_*2469del
ENST00000585748.3:c.737-246_737-241del	ENSP00000477641.2:n.737-246_737-241del
ENST00000585851.2:c.935-246_935-241del	ENSP00000467912.2:n.935-246_935-241del
ENST00000326873.12:c.1109-246_1109-241del MANE Select	ENSP00000324856.6:n.1109-246_1109-241del
ENST00000326873.11:c.1109-246_1109-241del	ENSP00000324856.6:n.1109-246_1109-241del
ENST00000585465.2:n.2596_2601del
ENST00000586243.5:c.1109-246_1109-241del	ENSP00000467240.2:n.1109-246_1109-241del
ENST00000589152.5:n.1807-246_1807-241del
NM_000455.4:c.1109-246_1109-241del , LRG_319t1:c.1109-246_1109-241del	NP_000446.1:n.1109-246_1109-241del
XM_005259617.1:c.1109-251_1109-246del	XP_005259674.1:n.1109-251_1109-246del
XM_011528209.1:c.887-251_887-246del	XP_011526511.1:n.887-251_887-246del
XM_005259617.3:c.1109-251_1109-246del	XP_005259674.1:n.1109-251_1109-246del
XM_011528209.2:c.887-251_887-246del	XP_011526511.1:n.887-251_887-246del
XR_001753738.2:n.1915-246_1915-241del
XR_001753740.2:n.1885-246_1885-241del
NM_000455.5:c.1109-246_1109-241del MANE Select	NP_000446.1:n.1109-246_1109-241del