Canonical Allele Identifier: CA2582592929

Gene: STK11

Linked Data

• dbSNP Id: rs2145424831
• gnomAD v4: 19-1220531-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220531G>T , CM000681.2:g.1220531G>T	GRCh38
NC_000019.9:g.1220530G>T , CM000681.1:g.1220530G>T	GRCh37
NC_000019.8:g.1171530G>T	NCBI36
NG_007460.2:g.36125G>T , LRG_319:g.36125G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.597+26G>T	ENSP00000490268.2:n.597+26G>T
ENST00000585748.3:c.225+26G>T	ENSP00000477641.2:n.225+26G>T
ENST00000585851.2:c.423+26G>T	ENSP00000467912.2:n.423+26G>T
ENST00000326873.12:c.597+26G>T MANE Select	ENSP00000324856.6:n.597+26G>T
ENST00000652231.1:c.597+26G>T	ENSP00000498804.1:n.597+26G>T
ENST00000326873.11:c.597+26G>T	ENSP00000324856.6:n.597+26G>T
ENST00000585851.1:c.423+26G>T	ENSP00000467912.1:n.423+26G>T
ENST00000586243.5:c.597+26G>T	ENSP00000467240.2:n.597+26G>T
ENST00000586358.5:n.446G>T
ENST00000589152.5:n.687+26G>T
ENST00000591133.2:n.519G>T
NM_000455.4:c.597+26G>T , LRG_319t1:c.597+26G>T	NP_000446.1:n.597+26G>T
XM_005259617.1:c.597+26G>T	XP_005259674.1:n.597+26G>T
XM_005259618.3:c.597+26G>T	XP_005259675.1:n.597+26G>T
XM_011528209.1:c.375+26G>T	XP_011526511.1:n.375+26G>T
XR_936204.1:n.1222+26G>T
XM_005259617.3:c.597+26G>T	XP_005259674.1:n.597+26G>T
XM_011528209.2:c.375+26G>T	XP_011526511.1:n.375+26G>T
XR_001753738.2:n.1222+26G>T
XR_001753739.1:n.1222+26G>T
XR_001753740.2:n.1222+26G>T
NM_000455.5:c.597+26G>T MANE Select	NP_000446.1:n.597+26G>T