Canonical Allele Identifier: CA631031769

Gene: STK11

Linked Data

• dbSNP Id: rs1226440550
• gnomAD v2: 19-1218684-G-GGCCCTGA
• gnomAD v3: 19-1218685-G-GGCCCTGA
• gnomAD v4: 19-1218685-G-GGCCCTGA
• MyVariant Identifiers: chr19:g.1218684_1218685insGCCCTGA (hg19) ; chr19:g.1218685_1218686insGCCCTGA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1218692_1218698dup , CM000681.2:g.1218692_1218698dup	GRCh38
NC_000019.9:g.1218691_1218697dup , CM000681.1:g.1218691_1218697dup	GRCh37
NC_000019.8:g.1169691_1169697dup	NCBI36
NG_007460.2:g.34286_34292dup , LRG_319:g.34286_34292dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.374+192_374+198dup	ENSP00000490268.2:n.374+192_374+198dup
ENST00000585748.3:c.2+192_2+198dup	ENSP00000477641.2:n.2+192_2+198dup
ENST00000585851.2:c.291-1681_291-1675dup	ENSP00000467912.2:n.291-1681_291-1675dup
ENST00000326873.12:c.374+192_374+198dup MANE Select	ENSP00000324856.6:n.374+192_374+198dup
ENST00000652231.1:c.374+192_374+198dup	ENSP00000498804.1:n.374+192_374+198dup
ENST00000326873.11:c.374+192_374+198dup	ENSP00000324856.6:n.374+192_374+198dup
ENST00000585748.2:c.2+192_2+198dup	ENSP00000477641.1:n.2+192_2+198dup
ENST00000585851.1:c.291-1681_291-1675dup	ENSP00000467912.1:n.291-1681_291-1675dup
ENST00000586243.5:c.374+192_374+198dup	ENSP00000467240.2:n.374+192_374+198dup
ENST00000586358.5:n.197+192_197+198dup
ENST00000589152.5:n.464+192_464+198dup
ENST00000593219.5:c.*199+192_*199+198dup	ENSP00000466610.1:n.*199+192_*199+198dup
NM_000455.4:c.374+192_374+198dup , LRG_319t1:c.374+192_374+198dup	NP_000446.1:n.374+192_374+198dup
XM_005259617.1:c.374+192_374+198dup	XP_005259674.1:n.374+192_374+198dup
XM_005259618.3:c.374+192_374+198dup	XP_005259675.1:n.374+192_374+198dup
XM_011528209.1:c.152+192_152+198dup	XP_011526511.1:n.152+192_152+198dup
XR_936204.1:n.999+192_999+198dup
XM_005259617.3:c.374+192_374+198dup	XP_005259674.1:n.374+192_374+198dup
XM_011528209.2:c.152+192_152+198dup	XP_011526511.1:n.152+192_152+198dup
XR_001753738.2:n.999+192_999+198dup
XR_001753739.1:n.999+192_999+198dup
XR_001753740.2:n.999+192_999+198dup
NM_000455.5:c.374+192_374+198dup MANE Select	NP_000446.1:n.374+192_374+198dup