Canonical Allele Identifier: CA2317589352

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219702_1219703delinsCG , CM000681.2:g.1219702_1219703delinsCG	GRCh38
NC_000019.9:g.1219701_1219702delinsCG , CM000681.1:g.1219701_1219702delinsCG	GRCh37
NC_000019.8:g.1170701_1170702delinsCG	NCBI36
NG_007460.2:g.35296_35297delinsCG , LRG_319:g.35296_35297delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+289_464+290delinsCG	ENSP00000490268.2:n.464+289_464+290delinsCG
ENST00000585748.3:c.92+289_92+290delinsCG	ENSP00000477641.2:n.92+289_92+290delinsCG
ENST00000585851.2:c.291-671_291-670delinsCG	ENSP00000467912.2:n.291-671_291-670delinsCG
ENST00000326873.12:c.464+289_464+290delinsCG MANE Select	ENSP00000324856.6:n.464+289_464+290delinsCG
ENST00000652231.1:c.464+289_464+290delinsCG	ENSP00000498804.1:n.464+289_464+290delinsCG
ENST00000326873.11:c.464+289_464+290delinsCG	ENSP00000324856.6:n.464+289_464+290delinsCG
ENST00000585851.1:c.291-671_291-670delinsCG	ENSP00000467912.1:n.291-671_291-670delinsCG
ENST00000586243.5:c.464+289_464+290delinsCG	ENSP00000467240.2:n.464+289_464+290delinsCG
ENST00000586358.5:n.287+289_287+290delinsCG
ENST00000589152.5:n.554+289_554+290delinsCG
NM_000455.4:c.464+289_464+290delinsCG , LRG_319t1:c.464+289_464+290delinsCG	NP_000446.1:n.464+289_464+290delinsCG
XM_005259617.1:c.464+289_464+290delinsCG	XP_005259674.1:n.464+289_464+290delinsCG
XM_005259618.3:c.464+289_464+290delinsCG	XP_005259675.1:n.464+289_464+290delinsCG
XM_011528209.1:c.242+289_242+290delinsCG	XP_011526511.1:n.242+289_242+290delinsCG
XR_936204.1:n.1089+289_1089+290delinsCG
XM_005259617.3:c.464+289_464+290delinsCG	XP_005259674.1:n.464+289_464+290delinsCG
XM_011528209.2:c.242+289_242+290delinsCG	XP_011526511.1:n.242+289_242+290delinsCG
XR_001753738.2:n.1089+289_1089+290delinsCG
XR_001753739.1:n.1089+289_1089+290delinsCG
XR_001753740.2:n.1089+289_1089+290delinsCG
NM_000455.5:c.464+289_464+290delinsCG MANE Select	NP_000446.1:n.464+289_464+290delinsCG