Canonical Allele Identifier: CA10577601

Gene: STK11

Linked Data

• ClinVar Variation Id: 234785
• ClinVar RCV Id: RCV000215979
• dbSNP Id: rs876661216
• MyVariant Identifiers: chr19:g.1226606_1226607del (hg19) ; chr19:g.1226607_1226608del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226607_1226608del , CM000681.2:g.1226607_1226608del	GRCh38
NC_000019.9:g.1226606_1226607del , CM000681.1:g.1226606_1226607del	GRCh37
NC_000019.8:g.1177606_1177607del	NCBI36
NG_007460.2:g.42201_42202del , LRG_319:g.42201_42202del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2863_*2864del	ENSP00000490268.2:n.*2863_*2864del
ENST00000585748.3:c.890_891del	ENSP00000477641.2:p.Ser297LysfsTer?
ENST00000585851.2:c.1088_1089del	ENSP00000467912.2:p.Ser363LysfsTer?
ENST00000326873.12:c.1262_1263del MANE Select	ENSP00000324856.6:p.Ser421LysfsTer?
ENST00000326873.11:c.1262_1263del	ENSP00000324856.6:p.Ser421LysfsTer?
ENST00000585465.2:n.2995_2996del
ENST00000586243.5:c.1259_1260del	ENSP00000467240.2:p.Ser420LysfsTer?
ENST00000589152.5:n.1960_1961del
NM_000455.4:c.1262_1263del , LRG_319t1:c.1262_1263del	NP_000446.1:p.Ser421LysfsTer?
XM_005259617.1:c.1257_1258del	XP_005259674.1:p.Gln420AlafsTer?
XM_011528209.1:c.1035_1036del	XP_011526511.1:p.Gln346AlafsTer?
XM_005259617.3:c.1257_1258del	XP_005259674.1:p.Gln420AlafsTer?
XM_011528209.2:c.1035_1036del	XP_011526511.1:p.Gln346AlafsTer?
XR_001753738.2:n.2068_2069del
XR_001753740.2:n.2038_2039del
NM_000455.5:c.1262_1263del MANE Select	NP_000446.1:p.Ser421LysfsTer?