Canonical Allele Identifier: CA2582592091

Gene: STK11

Linked Data

• gnomAD v4: 19-1219423-CGGGGCAGGGGCCAGGGTGGGGCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219429_1219451del , CM000681.2:g.1219429_1219451del	GRCh38
NC_000019.9:g.1219428_1219450del , CM000681.1:g.1219428_1219450del	GRCh37
NC_000019.8:g.1170428_1170450del	NCBI36
NG_007460.2:g.35023_35045del , LRG_319:g.35023_35045del

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.464+16_464+38del	ENSP00000490268.2:n.464+16_464+38del
ENST00000585748.3:c.92+16_92+38del	ENSP00000477641.2:n.92+16_92+38del
ENST00000585851.2:c.291-944_291-922del	ENSP00000467912.2:n.291-944_291-922del
ENST00000326873.12:c.464+16_464+38del MANE Select	ENSP00000324856.6:n.464+16_464+38del
ENST00000652231.1:c.464+16_464+38del	ENSP00000498804.1:n.464+16_464+38del
ENST00000326873.11:c.464+16_464+38del	ENSP00000324856.6:n.464+16_464+38del
ENST00000585851.1:c.291-944_291-922del	ENSP00000467912.1:n.291-944_291-922del
ENST00000586243.5:c.464+16_464+38del	ENSP00000467240.2:n.464+16_464+38del
ENST00000586358.5:n.287+16_287+38del
ENST00000589152.5:n.554+16_554+38del
NM_000455.4:c.464+16_464+38del , LRG_319t1:c.464+16_464+38del	NP_000446.1:n.464+16_464+38del
XM_005259617.1:c.464+16_464+38del	XP_005259674.1:n.464+16_464+38del
XM_005259618.3:c.464+16_464+38del	XP_005259675.1:n.464+16_464+38del
XM_011528209.1:c.242+16_242+38del	XP_011526511.1:n.242+16_242+38del
XR_936204.1:n.1089+16_1089+38del
XM_005259617.3:c.464+16_464+38del	XP_005259674.1:n.464+16_464+38del
XM_011528209.2:c.242+16_242+38del	XP_011526511.1:n.242+16_242+38del
XR_001753738.2:n.1089+16_1089+38del
XR_001753739.1:n.1089+16_1089+38del
XR_001753740.2:n.1089+16_1089+38del
NM_000455.5:c.464+16_464+38del MANE Select	NP_000446.1:n.464+16_464+38del