Canonical Allele Identifier: CA2695227839

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1206931_1206932delinsAT , CM000681.2:g.1206931_1206932delinsAT	GRCh38
NC_000019.9:g.1206930_1206931delinsAT , CM000681.1:g.1206930_1206931delinsAT	GRCh37
NC_000019.8:g.1157930_1157931delinsAT	NCBI36
NG_007460.2:g.22525_22526delinsAT , LRG_319:g.22525_22526delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.18_19delinsAT	ENSP00000490268.2:p.Pro7Ter
ENST00000585748.3:c.-82-11486_-82-11485delinsAT	ENSP00000477641.2:n.-82-11486_-82-11485delinsAT
ENST00000585851.2:c.18_19delinsAT	ENSP00000467912.2:p.Pro7Ter
ENST00000326873.12:c.18_19delinsAT MANE Select	ENSP00000324856.6:p.Pro7Ter
ENST00000652231.1:c.18_19delinsAT	ENSP00000498804.1:p.Pro7Ter
ENST00000326873.11:c.18_19delinsAT	ENSP00000324856.6:p.Pro7Ter
ENST00000585748.2:c.-82-11486_-82-11485delinsAT	ENSP00000477641.1:n.-82-11486_-82-11485delinsAT
ENST00000585851.1:c.18_19delinsAT	ENSP00000467912.1:p.Pro7Ter
ENST00000586243.5:c.18_19delinsAT	ENSP00000467240.2:p.Pro7Ter
ENST00000589152.5:n.108_109delinsAT
ENST00000593219.5:c.18_19delinsAT	ENSP00000466610.1:p.Pro7Ter
NM_000455.4:c.18_19delinsAT , LRG_319t1:c.18_19delinsAT	NP_000446.1:p.Pro7Ter
XM_005259617.1:c.18_19delinsAT	XP_005259674.1:p.Pro7Ter
XM_005259618.3:c.18_19delinsAT	XP_005259675.1:p.Pro7Ter
XM_011528209.1:c.-336_-335delinsAT	XP_011526511.1:n.-336_-335delinsAT
XR_936204.1:n.643_644delinsAT
XM_005259617.3:c.18_19delinsAT	XP_005259674.1:p.Pro7Ter
XM_011528209.2:c.-336_-335delinsAT	XP_011526511.1:n.-336_-335delinsAT
XR_001753738.2:n.643_644delinsAT
XR_001753739.1:n.643_644delinsAT
XR_001753740.2:n.643_644delinsAT
NM_000455.5:c.18_19delinsAT MANE Select	NP_000446.1:p.Pro7Ter