Canonical Allele Identifier: CA304025060

Gene: STK11

Linked Data

• dbSNP Id: rs869127541
• gnomAD v2: 19-1219444-C-CGGGGGCT
• gnomAD v3: 19-1219445-C-CGGGGGCT
• gnomAD v4: 19-1219445-C-CGGGGGCT
• MyVariant Identifiers: chr19:g.1219444_1219445insGGGGGCT (hg19) ; chr19:g.1219445_1219446insGGGGGCT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219451_1219452insTGGGGGC , CM000681.2:g.1219451_1219452insTGGGGGC	GRCh38
NC_000019.9:g.1219450_1219451insTGGGGGC , CM000681.1:g.1219450_1219451insTGGGGGC	GRCh37
NC_000019.8:g.1170450_1170451insTGGGGGC	NCBI36
NG_007460.2:g.35045_35046insTGGGGGC , LRG_319:g.35045_35046insTGGGGGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+38_464+39insTGGGGGC	ENSP00000490268.2:n.464+38_464+39insTGGGGGC
ENST00000585748.3:c.92+38_92+39insTGGGGGC	ENSP00000477641.2:n.92+38_92+39insTGGGGGC
ENST00000585851.2:c.291-922_291-921insTGGGGGC	ENSP00000467912.2:n.291-922_291-921insTGGGGGC
ENST00000326873.12:c.464+38_464+39insTGGGGGC MANE Select	ENSP00000324856.6:n.464+38_464+39insTGGGGGC
ENST00000652231.1:c.464+38_464+39insTGGGGGC	ENSP00000498804.1:n.464+38_464+39insTGGGGGC
ENST00000326873.11:c.464+38_464+39insTGGGGGC	ENSP00000324856.6:n.464+38_464+39insTGGGGGC
ENST00000585851.1:c.291-922_291-921insTGGGGGC	ENSP00000467912.1:n.291-922_291-921insTGGGGGC
ENST00000586243.5:c.464+38_464+39insTGGGGGC	ENSP00000467240.2:n.464+38_464+39insTGGGGGC
ENST00000586358.5:n.287+38_287+39insTGGGGGC
ENST00000589152.5:n.554+38_554+39insTGGGGGC
NM_000455.4:c.464+38_464+39insTGGGGGC , LRG_319t1:c.464+38_464+39insTGGGGGC	NP_000446.1:n.464+38_464+39insTGGGGGC
XM_005259617.1:c.464+38_464+39insTGGGGGC	XP_005259674.1:n.464+38_464+39insTGGGGGC
XM_005259618.3:c.464+38_464+39insTGGGGGC	XP_005259675.1:n.464+38_464+39insTGGGGGC
XM_011528209.1:c.242+38_242+39insTGGGGGC	XP_011526511.1:n.242+38_242+39insTGGGGGC
XR_936204.1:n.1089+38_1089+39insTGGGGGC
XM_005259617.3:c.464+38_464+39insTGGGGGC	XP_005259674.1:n.464+38_464+39insTGGGGGC
XM_011528209.2:c.242+38_242+39insTGGGGGC	XP_011526511.1:n.242+38_242+39insTGGGGGC
XR_001753738.2:n.1089+38_1089+39insTGGGGGC
XR_001753739.1:n.1089+38_1089+39insTGGGGGC
XR_001753740.2:n.1089+38_1089+39insTGGGGGC
NM_000455.5:c.464+38_464+39insTGGGGGC MANE Select	NP_000446.1:n.464+38_464+39insTGGGGGC