Canonical Allele Identifier: CA2582593262

Gene: STK11

Linked Data

• gnomAD v4: 19-1221462-CTGAGTGGAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1221463_1221471del , CM000681.2:g.1221463_1221471del	GRCh38
NC_000019.9:g.1221462_1221470del , CM000681.1:g.1221462_1221470del	GRCh37
NC_000019.8:g.1172462_1172470del	NCBI36
NG_007460.2:g.37057_37065del , LRG_319:g.37057_37065del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000585465.3:c.862+123_862+131del	ENSP00000490268.2:n.862+123_862+131del
ENST00000585748.3:c.490+123_490+131del	ENSP00000477641.2:n.490+123_490+131del
ENST00000585851.2:c.688+123_688+131del	ENSP00000467912.2:n.688+123_688+131del
ENST00000326873.12:c.862+123_862+131del MANE Select	ENSP00000324856.6:n.862+123_862+131del
ENST00000652231.1:c.862+123_862+131del	ENSP00000498804.1:n.862+123_862+131del
ENST00000326873.11:c.862+123_862+131del	ENSP00000324856.6:n.862+123_862+131del
ENST00000586243.5:c.862+123_862+131del	ENSP00000467240.2:n.862+123_862+131del
ENST00000586358.5:n.760+123_760+131del
ENST00000589152.5:n.1075_1083del
ENST00000591133.2:n.833+123_833+131del
NM_000455.4:c.862+123_862+131del , LRG_319t1:c.862+123_862+131del	NP_000446.1:n.862+123_862+131del
XM_005259617.1:c.862+123_862+131del	XP_005259674.1:n.862+123_862+131del
XM_005259618.3:c.862+123_862+131del	XP_005259675.1:n.862+123_862+131del
XM_011528209.1:c.640+123_640+131del	XP_011526511.1:n.640+123_640+131del
XR_936204.1:n.1487+123_1487+131del
XM_005259617.3:c.862+123_862+131del	XP_005259674.1:n.862+123_862+131del
XM_011528209.2:c.640+123_640+131del	XP_011526511.1:n.640+123_640+131del
XR_001753738.2:n.1487+123_1487+131del
XR_001753739.1:n.1487+123_1487+131del
XR_001753740.2:n.1487+123_1487+131del
NM_000455.5:c.862+123_862+131del MANE Select	NP_000446.1:n.862+123_862+131del