Canonical Allele Identifier: CA2582592081

Gene: STK11

Linked Data

• gnomAD v4: 19-1219417-C-CCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219417_1219418insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT , CM000681.2:g.1219417_1219418insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	GRCh38
NC_000019.9:g.1219416_1219417insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT , CM000681.1:g.1219416_1219417insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	GRCh37
NC_000019.8:g.1170416_1170417insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	NCBI36
NG_007460.2:g.35011_35012insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT , LRG_319:g.35011_35012insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	ENSP00000490268.2:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAG...
ENST00000585748.3:c.92+4_92+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	ENSP00000477641.2:n.92+4_92+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGA...
ENST00000585851.2:c.291-956_291-955insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	ENSP00000467912.2:n.291-956_291-955insCCTGCTCCTCTTCCCGTCTCCTT...
ENST00000326873.12:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT MANE Select	ENSP00000324856.6:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAG...
ENST00000652231.1:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	ENSP00000498804.1:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAG...
ENST00000326873.11:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	ENSP00000324856.6:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAG...
ENST00000585851.1:c.291-956_291-955insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	ENSP00000467912.1:n.291-956_291-955insCCTGCTCCTCTTCCCGTCTCCTT...
ENST00000586243.5:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	ENSP00000467240.2:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAG...
ENST00000586358.5:n.287+4_287+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT
ENST00000589152.5:n.554+4_554+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT
NM_000455.4:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT , LRG_319t1:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	NP_000446.1:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT...
XM_005259617.1:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	XP_005259674.1:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAG...
XM_005259618.3:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	XP_005259675.1:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAG...
XM_011528209.1:c.242+4_242+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	XP_011526511.1:n.242+4_242+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAG...
XR_936204.1:n.1089+4_1089+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT
XM_005259617.3:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	XP_005259674.1:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAG...
XM_011528209.2:c.242+4_242+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT	XP_011526511.1:n.242+4_242+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAG...
XR_001753738.2:n.1089+4_1089+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT
XR_001753739.1:n.1089+4_1089+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT
XR_001753740.2:n.1089+4_1089+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT
NM_000455.5:c.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT MANE Select	NP_000446.1:n.464+4_464+5insCCTGCTCCTCTTCCCGTCTCCTTGAAGGAGACT...