Canonical Allele Identifier: CA2582592098

Gene: STK11

Linked Data

• gnomAD v4: 19-1219429-AGGGGCCAGGGTGGGGCGGGGGCCG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219439_1219462del , CM000681.2:g.1219439_1219462del	GRCh38
NC_000019.9:g.1219438_1219461del , CM000681.1:g.1219438_1219461del	GRCh37
NC_000019.8:g.1170438_1170461del	NCBI36
NG_007460.2:g.35033_35056del , LRG_319:g.35033_35056del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+26_464+49del	ENSP00000490268.2:n.464+26_464+49del
ENST00000585748.3:c.92+26_92+49del	ENSP00000477641.2:n.92+26_92+49del
ENST00000585851.2:c.291-934_291-911del	ENSP00000467912.2:n.291-934_291-911del
ENST00000326873.12:c.464+26_464+49del MANE Select	ENSP00000324856.6:n.464+26_464+49del
ENST00000652231.1:c.464+26_464+49del	ENSP00000498804.1:n.464+26_464+49del
ENST00000326873.11:c.464+26_464+49del	ENSP00000324856.6:n.464+26_464+49del
ENST00000585851.1:c.291-934_291-911del	ENSP00000467912.1:n.291-934_291-911del
ENST00000586243.5:c.464+26_464+49del	ENSP00000467240.2:n.464+26_464+49del
ENST00000586358.5:n.287+26_287+49del
ENST00000589152.5:n.554+26_554+49del
NM_000455.4:c.464+26_464+49del , LRG_319t1:c.464+26_464+49del	NP_000446.1:n.464+26_464+49del
XM_005259617.1:c.464+26_464+49del	XP_005259674.1:n.464+26_464+49del
XM_005259618.3:c.464+26_464+49del	XP_005259675.1:n.464+26_464+49del
XM_011528209.1:c.242+26_242+49del	XP_011526511.1:n.242+26_242+49del
XR_936204.1:n.1089+26_1089+49del
XM_005259617.3:c.464+26_464+49del	XP_005259674.1:n.464+26_464+49del
XM_011528209.2:c.242+26_242+49del	XP_011526511.1:n.242+26_242+49del
XR_001753738.2:n.1089+26_1089+49del
XR_001753739.1:n.1089+26_1089+49del
XR_001753740.2:n.1089+26_1089+49del
NM_000455.5:c.464+26_464+49del MANE Select	NP_000446.1:n.464+26_464+49del