Canonical Allele Identifier: CA304025868

Gene: STK11

Linked Data

• ClinVar Variation Id: 1392824
• ClinVar RCV Id: RCV001882277
• dbSNP Id: rs897087953
• MyVariant Identifiers: chr19:g.1220384G>C (hg19) ; chr19:g.1220385G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1220385G>C , CM000681.2:g.1220385G>C	GRCh38
NC_000019.9:g.1220384G>C , CM000681.1:g.1220384G>C	GRCh37
NC_000019.8:g.1171384G>C	NCBI36
NG_007460.2:g.35979G>C , LRG_319:g.35979G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.477G>C	ENSP00000490268.2:p.Gln159His
ENST00000585748.3:c.105G>C	ENSP00000477641.2:p.Gln35His
ENST00000585851.2:c.303G>C	ENSP00000467912.2:p.Gln101His
ENST00000326873.12:c.477G>C MANE Select	ENSP00000324856.6:p.Gln159His
ENST00000652231.1:c.477G>C	ENSP00000498804.1:p.Gln159His
ENST00000326873.11:c.477G>C	ENSP00000324856.6:p.Gln159His
ENST00000585851.1:c.303G>C	ENSP00000467912.1:p.Gln101His
ENST00000586243.5:c.477G>C	ENSP00000467240.2:p.Gln159His
ENST00000586358.5:n.300G>C
ENST00000589152.5:n.567G>C
ENST00000591133.2:n.373G>C
NM_000455.4:c.477G>C , LRG_319t1:c.477G>C	NP_000446.1:p.Gln159His
XM_005259617.1:c.477G>C	XP_005259674.1:p.Gln159His
XM_005259618.3:c.477G>C	XP_005259675.1:p.Gln159His
XM_011528209.1:c.255G>C	XP_011526511.1:p.Gln85His
XR_936204.1:n.1102G>C
XM_005259617.3:c.477G>C	XP_005259674.1:p.Gln159His
XM_011528209.2:c.255G>C	XP_011526511.1:p.Gln85His
XR_001753738.2:n.1102G>C
XR_001753739.1:n.1102G>C
XR_001753740.2:n.1102G>C
NM_000455.5:c.477G>C MANE Select	NP_000446.1:p.Gln159His