Canonical Allele Identifier: CA2581945966

Gene: STK11

Linked Data

• gnomAD v3: 19-1219552-G-GTTTTTTT
• gnomAD v4: 19-1219552-G-GTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219553_1219554insTTTTTTT , CM000681.2:g.1219553_1219554insTTTTTTT	GRCh38
NC_000019.9:g.1219552_1219553insTTTTTTT , CM000681.1:g.1219552_1219553insTTTTTTT	GRCh37
NC_000019.8:g.1170552_1170553insTTTTTTT	NCBI36
NG_007460.2:g.35147_35148insTTTTTTT , LRG_319:g.35147_35148insTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+140_464+141insTTTTTTT	ENSP00000490268.2:n.464+140_464+141insTTTTTTT
ENST00000585748.3:c.92+140_92+141insTTTTTTT	ENSP00000477641.2:n.92+140_92+141insTTTTTTT
ENST00000585851.2:c.291-820_291-819insTTTTTTT	ENSP00000467912.2:n.291-820_291-819insTTTTTTT
ENST00000326873.12:c.464+140_464+141insTTTTTTT MANE Select	ENSP00000324856.6:n.464+140_464+141insTTTTTTT
ENST00000652231.1:c.464+140_464+141insTTTTTTT	ENSP00000498804.1:n.464+140_464+141insTTTTTTT
ENST00000326873.11:c.464+140_464+141insTTTTTTT	ENSP00000324856.6:n.464+140_464+141insTTTTTTT
ENST00000585851.1:c.291-820_291-819insTTTTTTT	ENSP00000467912.1:n.291-820_291-819insTTTTTTT
ENST00000586243.5:c.464+140_464+141insTTTTTTT	ENSP00000467240.2:n.464+140_464+141insTTTTTTT
ENST00000586358.5:n.287+140_287+141insTTTTTTT
ENST00000589152.5:n.554+140_554+141insTTTTTTT
NM_000455.4:c.464+140_464+141insTTTTTTT , LRG_319t1:c.464+140_464+141insTTTTTTT	NP_000446.1:n.464+140_464+141insTTTTTTT
XM_005259617.1:c.464+140_464+141insTTTTTTT	XP_005259674.1:n.464+140_464+141insTTTTTTT
XM_005259618.3:c.464+140_464+141insTTTTTTT	XP_005259675.1:n.464+140_464+141insTTTTTTT
XM_011528209.1:c.242+140_242+141insTTTTTTT	XP_011526511.1:n.242+140_242+141insTTTTTTT
XR_936204.1:n.1089+140_1089+141insTTTTTTT
XM_005259617.3:c.464+140_464+141insTTTTTTT	XP_005259674.1:n.464+140_464+141insTTTTTTT
XM_011528209.2:c.242+140_242+141insTTTTTTT	XP_011526511.1:n.242+140_242+141insTTTTTTT
XR_001753738.2:n.1089+140_1089+141insTTTTTTT
XR_001753739.1:n.1089+140_1089+141insTTTTTTT
XR_001753740.2:n.1089+140_1089+141insTTTTTTT
NM_000455.5:c.464+140_464+141insTTTTTTT MANE Select	NP_000446.1:n.464+140_464+141insTTTTTTT