Canonical Allele Identifier: CA504892393

Gene: STK11

Linked Data

• ClinVar Variation Id: 1104445
• ClinVar RCV Id: RCV001428496 ; RCV001526275
• dbSNP Id: rs2145425219
• gnomAD v4: 19-1220637-T-A
• MyVariant Identifiers: chr19:g.1220636T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220637T>A , CM000681.2:g.1220637T>A	GRCh38
NC_000019.9:g.1220636T>A , CM000681.1:g.1220636T>A	GRCh37
NC_000019.8:g.1171636T>A	NCBI36
NG_007460.2:g.36231T>A , LRG_319:g.36231T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.654T>A	ENSP00000490268.2:p.Ala218=
ENST00000585748.3:c.282T>A	ENSP00000477641.2:p.Ala94=
ENST00000585851.2:c.480T>A	ENSP00000467912.2:p.Ala160=
ENST00000326873.12:c.654T>A MANE Select	ENSP00000324856.6:p.Ala218=
ENST00000652231.1:c.654T>A	ENSP00000498804.1:p.Ala218=
ENST00000326873.11:c.654T>A	ENSP00000324856.6:p.Ala218=
ENST00000586243.5:c.654T>A	ENSP00000467240.2:p.Ala218=
ENST00000586358.5:n.552T>A
ENST00000589152.5:n.744T>A
ENST00000591133.2:n.625T>A
NM_000455.4:c.654T>A , LRG_319t1:c.654T>A	NP_000446.1:p.Ala218=
XM_005259617.1:c.654T>A	XP_005259674.1:p.Ala218=
XM_005259618.3:c.654T>A	XP_005259675.1:p.Ala218=
XM_011528209.1:c.432T>A	XP_011526511.1:p.Ala144=
XR_936204.1:n.1279T>A
XM_005259617.3:c.654T>A	XP_005259674.1:p.Ala218=
XM_011528209.2:c.432T>A	XP_011526511.1:p.Ala144=
XR_001753738.2:n.1279T>A
XR_001753739.1:n.1279T>A
XR_001753740.2:n.1279T>A
NM_000455.5:c.654T>A MANE Select	NP_000446.1:p.Ala218=