Canonical Allele Identifier: CA2582597116

Gene: STK11

Linked Data

• gnomAD v4: 19-1226616-T-TCCG

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226620_1226622dup , CM000681.2:g.1226620_1226622dup	GRCh38
NC_000019.9:g.1226619_1226621dup , CM000681.1:g.1226619_1226621dup	GRCh37
NC_000019.8:g.1177619_1177621dup	NCBI36
NG_007460.2:g.42214_42216dup , LRG_319:g.42214_42216dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2876_*2878dup	ENSP00000490268.2:n.*2876_*2878dup
ENST00000585748.3:c.903_905dup	ENSP00000477641.2:p.Arg302_Leu303insArg
ENST00000585851.2:c.1101_1103dup	ENSP00000467912.2:p.Arg368_Leu369insArg
ENST00000326873.12:c.1275_1277dup MANE Select	ENSP00000324856.6:p.Arg426_Leu427insArg
ENST00000326873.11:c.1275_1277dup	ENSP00000324856.6:p.Arg426_Leu427insArg
ENST00000585465.2:n.3008_3010dup
ENST00000586243.5:c.1272_1274dup	ENSP00000467240.2:p.Arg425_Leu426insArg
ENST00000589152.5:n.1973_1975dup
NM_000455.4:c.1275_1277dup , LRG_319t1:c.1275_1277dup	NP_000446.1:p.Arg426_Leu427insArg
XM_005259617.1:c.1270_1272dup	XP_005259674.1:p.Pro424_Ala425insPro
XM_011528209.1:c.1048_1050dup	XP_011526511.1:p.Pro350_Ala351insPro
XM_005259617.3:c.1270_1272dup	XP_005259674.1:p.Pro424_Ala425insPro
XM_011528209.2:c.1048_1050dup	XP_011526511.1:p.Pro350_Ala351insPro
XR_001753738.2:n.2081_2083dup
XR_001753740.2:n.2051_2053dup
NM_000455.5:c.1275_1277dup MANE Select	NP_000446.1:p.Arg426_Leu427insArg