Canonical Allele Identifier: CA2582592922

Gene: STK11

Linked Data

• gnomAD v4: 19-1220525-G-GGCCCTGGGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220530_1220539dup , CM000681.2:g.1220530_1220539dup	GRCh38
NC_000019.9:g.1220529_1220538dup , CM000681.1:g.1220529_1220538dup	GRCh37
NC_000019.8:g.1171529_1171538dup	NCBI36
NG_007460.2:g.36124_36133dup , LRG_319:g.36124_36133dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.597+25_597+34dup	ENSP00000490268.2:n.597+25_597+34dup
ENST00000585748.3:c.225+25_225+34dup	ENSP00000477641.2:n.225+25_225+34dup
ENST00000585851.2:c.423+25_423+34dup	ENSP00000467912.2:n.423+25_423+34dup
ENST00000326873.12:c.597+25_597+34dup MANE Select	ENSP00000324856.6:n.597+25_597+34dup
ENST00000652231.1:c.597+25_597+34dup	ENSP00000498804.1:n.597+25_597+34dup
ENST00000326873.11:c.597+25_597+34dup	ENSP00000324856.6:n.597+25_597+34dup
ENST00000585851.1:c.423+25_423+34dup	ENSP00000467912.1:n.423+25_423+34dup
ENST00000586243.5:c.597+25_597+34dup	ENSP00000467240.2:n.597+25_597+34dup
ENST00000586358.5:n.445_454dup
ENST00000589152.5:n.687+25_687+34dup
ENST00000591133.2:n.518_527dup
NM_000455.4:c.597+25_597+34dup , LRG_319t1:c.597+25_597+34dup	NP_000446.1:n.597+25_597+34dup
XM_005259617.1:c.597+25_597+34dup	XP_005259674.1:n.597+25_597+34dup
XM_005259618.3:c.597+25_597+34dup	XP_005259675.1:n.597+25_597+34dup
XM_011528209.1:c.375+25_375+34dup	XP_011526511.1:n.375+25_375+34dup
XR_936204.1:n.1222+25_1222+34dup
XM_005259617.3:c.597+25_597+34dup	XP_005259674.1:n.597+25_597+34dup
XM_011528209.2:c.375+25_375+34dup	XP_011526511.1:n.375+25_375+34dup
XR_001753738.2:n.1222+25_1222+34dup
XR_001753739.1:n.1222+25_1222+34dup
XR_001753740.2:n.1222+25_1222+34dup
NM_000455.5:c.597+25_597+34dup MANE Select	NP_000446.1:n.597+25_597+34dup