Canonical Allele Identifier: CA402953933

Gene: STK11

Linked Data

• gnomAD v4: 19-1226584-T-G
• MyVariant Identifiers: chr19:g.1226583T>G (hg19) ; chr19:g.1226584T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226584T>G , CM000681.2:g.1226584T>G	GRCh38
NC_000019.9:g.1226583T>G , CM000681.1:g.1226583T>G	GRCh37
NC_000019.8:g.1177583T>G	NCBI36
NG_007460.2:g.42178T>G , LRG_319:g.42178T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2840T>G	ENSP00000490268.2:n.*2840T>G
ENST00000585748.3:c.867T>G	ENSP00000477641.2:p.Pro289=
ENST00000585851.2:c.1065T>G	ENSP00000467912.2:p.Pro355=
ENST00000326873.12:c.1239T>G MANE Select	ENSP00000324856.6:p.Pro413=
ENST00000326873.11:c.1239T>G	ENSP00000324856.6:p.Pro413=
ENST00000585465.2:n.2972T>G
ENST00000586243.5:c.1238T>G	ENSP00000467240.2:p.Leu413Arg
ENST00000589152.5:n.1937T>G
NM_000455.4:c.1239T>G , LRG_319t1:c.1239T>G	NP_000446.1:p.Pro413=
XM_005259617.1:c.1234T>G	XP_005259674.1:p.Cys412Gly
XM_011528209.1:c.1012T>G	XP_011526511.1:p.Cys338Gly
XM_005259617.3:c.1234T>G	XP_005259674.1:p.Cys412Gly
XM_011528209.2:c.1012T>G	XP_011526511.1:p.Cys338Gly
XR_001753738.2:n.2045T>G
XR_001753740.2:n.2015T>G
NM_000455.5:c.1239T>G MANE Select	NP_000446.1:p.Pro413=