Canonical Allele Identifier: CA504892388

Gene: STK11

Linked Data

• MyVariant Identifiers: chr19:g.1220632_1220633insG (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220635dup , CM000681.2:g.1220635dup	GRCh38
NC_000019.9:g.1220634dup , CM000681.1:g.1220634dup	GRCh37
NC_000019.8:g.1171634dup	NCBI36
NG_007460.2:g.36229dup , LRG_319:g.36229dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000585465.3:c.652dup	ENSP00000490268.2:p.Ala218GlyfsTer?
ENST00000585748.3:c.280dup	ENSP00000477641.2:p.Ala94GlyfsTer?
ENST00000585851.2:c.478dup	ENSP00000467912.2:p.Ala160GlyfsTer?
ENST00000326873.12:c.652dup MANE Select	ENSP00000324856.6:p.Ala218GlyfsTer?
ENST00000652231.1:c.652dup	ENSP00000498804.1:p.Ala218GlyfsTer?
ENST00000326873.11:c.652dup	ENSP00000324856.6:p.Ala218GlyfsTer?
ENST00000586243.5:c.652dup	ENSP00000467240.2:p.Ala218GlyfsTer?
ENST00000586358.5:n.550dup
ENST00000589152.5:n.742dup
ENST00000591133.2:n.623dup
NM_000455.4:c.652dup , LRG_319t1:c.652dup	NP_000446.1:p.Ala218GlyfsTer?
XM_005259617.1:c.652dup	XP_005259674.1:p.Ala218GlyfsTer?
XM_005259618.3:c.652dup	XP_005259675.1:p.Ala218GlyfsTer?
XM_011528209.1:c.430dup	XP_011526511.1:p.Ala144GlyfsTer?
XR_936204.1:n.1277dup
XM_005259617.3:c.652dup	XP_005259674.1:p.Ala218GlyfsTer?
XM_011528209.2:c.430dup	XP_011526511.1:p.Ala144GlyfsTer?
XR_001753738.2:n.1277dup
XR_001753739.1:n.1277dup
XR_001753740.2:n.1277dup
NM_000455.5:c.652dup MANE Select	NP_000446.1:p.Ala218GlyfsTer?