Canonical Allele Identifier: CA2317593783

Gene: STK11

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1226609_1226610delinsAG , CM000681.2:g.1226609_1226610delinsAG	GRCh38
NC_000019.9:g.1226608_1226609delinsAG , CM000681.1:g.1226608_1226609delinsAG	GRCh37
NC_000019.8:g.1177608_1177609delinsAG	NCBI36
NG_007460.2:g.42203_42204delinsAG , LRG_319:g.42203_42204delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.*2865_*2866delinsAG	ENSP00000490268.2:n.*2865_*2866delinsAG
ENST00000585748.3:c.892_893delinsAG	ENSP00000477641.2:p.Ser298=
ENST00000585851.2:c.1090_1091delinsAG	ENSP00000467912.2:p.Ser364=
ENST00000326873.12:c.1264_1265delinsAG MANE Select	ENSP00000324856.6:p.Ser422=
ENST00000326873.11:c.1264_1265delinsAG	ENSP00000324856.6:p.Ser422=
ENST00000585465.2:n.2997_2998delinsAG
ENST00000586243.5:c.1261_1262delinsAG	ENSP00000467240.2:p.Ser421=
ENST00000589152.5:n.1962_1963delinsAG
NM_000455.4:c.1264_1265delinsAG , LRG_319t1:c.1264_1265delinsAG	NP_000446.1:p.Ser422=
XM_005259617.1:c.1259_1260delinsAG	XP_005259674.1:p.Gln420=
XM_011528209.1:c.1037_1038delinsAG	XP_011526511.1:p.Gln346=
XM_005259617.3:c.1259_1260delinsAG	XP_005259674.1:p.Gln420=
XM_011528209.2:c.1037_1038delinsAG	XP_011526511.1:p.Gln346=
XR_001753738.2:n.2070_2071delinsAG
XR_001753740.2:n.2040_2041delinsAG
NM_000455.5:c.1264_1265delinsAG MANE Select	NP_000446.1:p.Ser422=