Canonical Allele Identifier: CA1975973636

Gene: LPXN

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.58571651T>A , CM000673.2:g.58571651T>A	GRCh38
NC_000011.9:g.58339124T>A , CM000673.1:g.58339124T>A	GRCh37
NC_000011.8:g.58095700T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395074.7:c.14-938A>T MANE Select	ENSP00000378512.2:n.14-938A>T
ENST00000395074.6:c.14-938A>T	ENSP00000378512.2:n.14-938A>T
ENST00000528489.1:c.1-938A>T	ENSP00000461855.1:n.1-938A>T
ENST00000528954.5:c.29-938A>T	ENSP00000431284.1:n.29-938A>T
ENST00000529915.1:n.125-938A>T
ENST00000530561.5:c.14-938A>T	ENSP00000437094.1:n.14-938A>T
NM_001143995.1:c.29-938A>T	NP_001137467.1:n.29-938A>T
NM_001143995.2:c.29-938A>T	NP_001137467.1:n.29-938A>T
NM_001307951.1:c.1-938A>T	NP_001294880.1:n.1-938A>T
NM_004811.2:c.14-938A>T	NP_004802.1:n.14-938A>T
XM_006718750.1:c.-275-938A>T	XP_006718813.1:n.-275-938A>T
XM_011545388.1:c.1-938A>T	XP_011543690.1:n.1-938A>T
XM_011545390.1:c.1-938A>T	XP_011543692.1:n.1-938A>T
XM_011545391.1:c.1-938A>T	XP_011543693.1:n.1-938A>T
XM_011545392.1:c.1-938A>T	XP_011543694.1:n.1-938A>T
XM_011545393.1:c.29-938A>T	XP_011543695.1:n.29-938A>T
XM_011545394.1:c.14-938A>T	XP_011543696.1:n.14-938A>T
XM_011545388.3:c.1-938A>T	XP_011543690.1:n.1-938A>T
XM_011545390.2:c.1-938A>T	XP_011543692.1:n.1-938A>T
XM_011545391.3:c.1-938A>T	XP_011543693.1:n.1-938A>T
XM_011545393.3:c.29-938A>T	XP_011543695.1:n.29-938A>T
XM_011545394.3:c.14-938A>T	XP_011543696.1:n.14-938A>T
XM_017018579.2:c.29-938A>T	XP_016874068.1:n.29-938A>T
NM_001143995.3:c.29-938A>T	NP_001137467.1:n.29-938A>T
NM_001307951.2:c.1-938A>T	NP_001294880.1:n.1-938A>T
NM_004811.3:c.14-938A>T MANE Select	NP_004802.1:n.14-938A>T