Canonical Allele Identifier: CA2132699

Gene: STK11IP

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.219608068C>T , CM000664.2:g.219608068C>T	GRCh38
NC_000002.11:g.220472790C>T , CM000664.1:g.220472790C>T	GRCh37
NC_000002.10:g.220181034C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_052902.4:c.1241C>T MANE Select	NP_443134.3:p.Pro414Leu
ENST00000456909.6:c.1241C>T MANE Select	ENSP00000389383.1:p.Pro414Leu
NM_052902.2:c.1274C>T	NP_443134.2:p.Pro425Leu
NM_052902.3:c.1241C>T	NP_443134.3:p.Pro414Leu
ENST00000295641.14:c.1274C>T	ENSP00000295641.10:p.Pro425Leu
ENST00000456909.5:c.1241C>T	ENSP00000389383.1:p.Pro414Leu
ENST00000475396.5:n.1222C>T
XM_011510526.1:c.1241C>T	XP_011508828.1:p.Pro414Leu
XM_011510527.1:c.1241C>T	XP_011508829.1:p.Pro414Leu
XM_011510527.3:c.1241C>T	XP_011508829.1:p.Pro414Leu
XM_011510528.1:c.176C>T	XP_011508830.1:p.Pro59Leu
XM_011510528.2:c.176C>T	XP_011508830.1:p.Pro59Leu
XM_011510529.1:c.1241C>T	XP_011508831.1:p.Pro414Leu
XR_002959068.1:n.1320C>T
XR_002959069.1:n.1699C>T
XR_427063.1:n.1320C>T
XR_922833.1:n.1320C>T
XR_922834.1:n.1320C>T
XR_922834.2:n.1320C>T
XR_922835.1:n.1320C>T
XR_922835.2:n.1320C>T