Canonical Allele Identifier: CA783333866

Gene: STK11

Linked Data

• dbSNP Id: rs914339046
• gnomAD v3: 19-1219528-G-GT
• gnomAD v4: 19-1219528-G-GT
• MyVariant Identifiers: chr19:g.1219527_1219528insT (hg19) ; chr19:g.1219528_1219529insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219535dup , CM000681.2:g.1219535dup	GRCh38
NC_000019.9:g.1219534dup , CM000681.1:g.1219534dup	GRCh37
NC_000019.8:g.1170534dup	NCBI36
NG_007460.2:g.35129dup , LRG_319:g.35129dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+122dup	ENSP00000490268.2:n.464+122dup
ENST00000585748.3:c.92+122dup	ENSP00000477641.2:n.92+122dup
ENST00000585851.2:c.291-838dup	ENSP00000467912.2:n.291-838dup
ENST00000326873.12:c.464+122dup MANE Select	ENSP00000324856.6:n.464+122dup
ENST00000652231.1:c.464+122dup	ENSP00000498804.1:n.464+122dup
ENST00000326873.11:c.464+122dup	ENSP00000324856.6:n.464+122dup
ENST00000585851.1:c.291-838dup	ENSP00000467912.1:n.291-838dup
ENST00000586243.5:c.464+122dup	ENSP00000467240.2:n.464+122dup
ENST00000586358.5:n.287+122dup
ENST00000589152.5:n.554+122dup
NM_000455.4:c.464+122dup , LRG_319t1:c.464+122dup	NP_000446.1:n.464+122dup
XM_005259617.1:c.464+122dup	XP_005259674.1:n.464+122dup
XM_005259618.3:c.464+122dup	XP_005259675.1:n.464+122dup
XM_011528209.1:c.242+122dup	XP_011526511.1:n.242+122dup
XR_936204.1:n.1089+122dup
XM_005259617.3:c.464+122dup	XP_005259674.1:n.464+122dup
XM_011528209.2:c.242+122dup	XP_011526511.1:n.242+122dup
XR_001753738.2:n.1089+122dup
XR_001753739.1:n.1089+122dup
XR_001753740.2:n.1089+122dup
NM_000455.5:c.464+122dup MANE Select	NP_000446.1:n.464+122dup