Canonical Allele Identifier: CA402953836

Gene: STK11

Linked Data

• gnomAD v4: 19-1226568-G-T
• MyVariant Identifiers: chr19:g.1226567G>T (hg19) ; chr19:g.1226568G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226568G>T , CM000681.2:g.1226568G>T	GRCh38
NC_000019.9:g.1226567G>T , CM000681.1:g.1226567G>T	GRCh37
NC_000019.8:g.1177567G>T	NCBI36
NG_007460.2:g.42162G>T , LRG_319:g.42162G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2824G>T	ENSP00000490268.2:n.*2824G>T
ENST00000585748.3:c.851G>T	ENSP00000477641.2:p.Gly284Val
ENST00000585851.2:c.1049G>T	ENSP00000467912.2:p.Gly350Val
ENST00000326873.12:c.1223G>T MANE Select	ENSP00000324856.6:p.Gly408Val
ENST00000326873.11:c.1223G>T	ENSP00000324856.6:p.Gly408Val
ENST00000585465.2:n.2956G>T
ENST00000586243.5:c.1222G>T	ENSP00000467240.2:p.Ala408Ser
ENST00000589152.5:n.1921G>T
NM_000455.4:c.1223G>T , LRG_319t1:c.1223G>T	NP_000446.1:p.Gly408Val
XM_005259617.1:c.1218G>T	XP_005259674.1:p.Gly406=
XM_011528209.1:c.996G>T	XP_011526511.1:p.Gly332=
XM_005259617.3:c.1218G>T	XP_005259674.1:p.Gly406=
XM_011528209.2:c.996G>T	XP_011526511.1:p.Gly332=
XR_001753738.2:n.2029G>T
XR_001753740.2:n.1999G>T
NM_000455.5:c.1223G>T MANE Select	NP_000446.1:p.Gly408Val