Canonical Allele Identifier: CA2573131817

Gene: STK11

Linked Data

• gnomAD v4: 19-1226573-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226578del , CM000681.2:g.1226578del	GRCh38
NC_000019.9:g.1226577del , CM000681.1:g.1226577del	GRCh37
NC_000019.8:g.1177577del	NCBI36
NG_007460.2:g.42172del , LRG_319:g.42172del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2834del	ENSP00000490268.2:n.*2834del
ENST00000585748.3:c.861del	ENSP00000477641.2:p.Asn288ThrfsTer?
ENST00000585851.2:c.1059del	ENSP00000467912.2:p.Asn354ThrfsTer?
ENST00000326873.12:c.1233del MANE Select	ENSP00000324856.6:p.Asn412ThrfsTer?
ENST00000326873.11:c.1233del	ENSP00000324856.6:p.Asn412ThrfsTer?
ENST00000585465.2:n.2966del
ENST00000586243.5:c.1232del	ENSP00000467240.2:p.Pro411GlnfsTer?
ENST00000589152.5:n.1931del
NM_000455.4:c.1233del , LRG_319t1:c.1233del	NP_000446.1:p.Asn412ThrfsTer?
XM_005259617.1:c.1228del	XP_005259674.1:p.Gln410AsnfsTer23
XM_011528209.1:c.1006del	XP_011526511.1:p.Gln336AsnfsTer23
XM_005259617.3:c.1228del	XP_005259674.1:p.Gln410AsnfsTer23
XM_011528209.2:c.1006del	XP_011526511.1:p.Gln336AsnfsTer23
XR_001753738.2:n.2039del
XR_001753740.2:n.2009del
NM_000455.5:c.1233del MANE Select	NP_000446.1:p.Asn412ThrfsTer?