Canonical Allele Identifier: CA2582592170

Gene: STK11

Linked Data

• gnomAD v4: 19-1219467-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1219467G>T , CM000681.2:g.1219467G>T	GRCh38
NC_000019.9:g.1219466G>T , CM000681.1:g.1219466G>T	GRCh37
NC_000019.8:g.1170466G>T	NCBI36
NG_007460.2:g.35061G>T , LRG_319:g.35061G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.464+54G>T	ENSP00000490268.2:n.464+54G>T
ENST00000585748.3:c.92+54G>T	ENSP00000477641.2:n.92+54G>T
ENST00000585851.2:c.291-906G>T	ENSP00000467912.2:n.291-906G>T
ENST00000326873.12:c.464+54G>T MANE Select	ENSP00000324856.6:n.464+54G>T
ENST00000652231.1:c.464+54G>T	ENSP00000498804.1:n.464+54G>T
ENST00000326873.11:c.464+54G>T	ENSP00000324856.6:n.464+54G>T
ENST00000585851.1:c.291-906G>T	ENSP00000467912.1:n.291-906G>T
ENST00000586243.5:c.464+54G>T	ENSP00000467240.2:n.464+54G>T
ENST00000586358.5:n.287+54G>T
ENST00000589152.5:n.554+54G>T
NM_000455.4:c.464+54G>T , LRG_319t1:c.464+54G>T	NP_000446.1:n.464+54G>T
XM_005259617.1:c.464+54G>T	XP_005259674.1:n.464+54G>T
XM_005259618.3:c.464+54G>T	XP_005259675.1:n.464+54G>T
XM_011528209.1:c.242+54G>T	XP_011526511.1:n.242+54G>T
XR_936204.1:n.1089+54G>T
XM_005259617.3:c.464+54G>T	XP_005259674.1:n.464+54G>T
XM_011528209.2:c.242+54G>T	XP_011526511.1:n.242+54G>T
XR_001753738.2:n.1089+54G>T
XR_001753739.1:n.1089+54G>T
XR_001753740.2:n.1089+54G>T
NM_000455.5:c.464+54G>T MANE Select	NP_000446.1:n.464+54G>T