Canonical Allele Identifier: CA2317589146

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219429_1219430delinsAG , CM000681.2:g.1219429_1219430delinsAG	GRCh38
NC_000019.9:g.1219428_1219429delinsAG , CM000681.1:g.1219428_1219429delinsAG	GRCh37
NC_000019.8:g.1170428_1170429delinsAG	NCBI36
NG_007460.2:g.35023_35024delinsAG , LRG_319:g.35023_35024delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+16_464+17delinsAG	ENSP00000490268.2:n.464+16_464+17delinsAG
ENST00000585748.3:c.92+16_92+17delinsAG	ENSP00000477641.2:n.92+16_92+17delinsAG
ENST00000585851.2:c.291-944_291-943delinsAG	ENSP00000467912.2:n.291-944_291-943delinsAG
ENST00000326873.12:c.464+16_464+17delinsAG MANE Select	ENSP00000324856.6:n.464+16_464+17delinsAG
ENST00000652231.1:c.464+16_464+17delinsAG	ENSP00000498804.1:n.464+16_464+17delinsAG
ENST00000326873.11:c.464+16_464+17delinsAG	ENSP00000324856.6:n.464+16_464+17delinsAG
ENST00000585851.1:c.291-944_291-943delinsAG	ENSP00000467912.1:n.291-944_291-943delinsAG
ENST00000586243.5:c.464+16_464+17delinsAG	ENSP00000467240.2:n.464+16_464+17delinsAG
ENST00000586358.5:n.287+16_287+17delinsAG
ENST00000589152.5:n.554+16_554+17delinsAG
NM_000455.4:c.464+16_464+17delinsAG , LRG_319t1:c.464+16_464+17delinsAG	NP_000446.1:n.464+16_464+17delinsAG
XM_005259617.1:c.464+16_464+17delinsAG	XP_005259674.1:n.464+16_464+17delinsAG
XM_005259618.3:c.464+16_464+17delinsAG	XP_005259675.1:n.464+16_464+17delinsAG
XM_011528209.1:c.242+16_242+17delinsAG	XP_011526511.1:n.242+16_242+17delinsAG
XR_936204.1:n.1089+16_1089+17delinsAG
XM_005259617.3:c.464+16_464+17delinsAG	XP_005259674.1:n.464+16_464+17delinsAG
XM_011528209.2:c.242+16_242+17delinsAG	XP_011526511.1:n.242+16_242+17delinsAG
XR_001753738.2:n.1089+16_1089+17delinsAG
XR_001753739.1:n.1089+16_1089+17delinsAG
XR_001753740.2:n.1089+16_1089+17delinsAG
NM_000455.5:c.464+16_464+17delinsAG MANE Select	NP_000446.1:n.464+16_464+17delinsAG