Canonical Allele Identifier: CA2692553076

Gene: LHX3

Linked Data

• gnomAD v4: 9-136197555-CG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197560del , CM000671.2:g.136197560del	GRCh38
NC_000009.11:g.139089406del , CM000671.1:g.139089406del	GRCh37
NC_000009.10:g.138229227del	NCBI36
NG_008097.1:g.12554del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.978del	ENSP00000360811.3:p.Ala327ProfsTer?
ENST00000371748.10:c.963del MANE Select	ENSP00000360813.4:p.Ala322ProfsTer?
ENST00000645419.1:n.1788del
ENST00000371746.7:c.978del	ENSP00000360811.3:p.Ala327ProfsTer?
ENST00000371748.9:c.963del	ENSP00000360813.4:p.Ala322ProfsTer?
ENST00000619587.1:c.930del	ENSP00000483080.1:p.Ala311ProfsTer?
NM_014564.3:c.978del	NP_055379.1:p.Ala327ProfsTer?
NM_178138.4:c.963del	NP_835258.1:p.Ala322ProfsTer?
XM_005263410.1:c.930del	XP_005263467.1:p.Ala311ProfsTer?
NM_001363746.1:c.930del	NP_001350675.1:p.Ala311ProfsTer?
NM_014564.4:c.978del	NP_055379.1:p.Ala327ProfsTer?
NM_178138.5:c.963del	NP_835258.1:p.Ala322ProfsTer?
XM_017015168.1:c.891del	XP_016870657.1:p.Ala298ProfsTer?
NM_178138.6:c.963del MANE Select	NP_835258.1:p.Ala322ProfsTer?
NM_014564.5:c.978del	NP_055379.1:p.Ala327ProfsTer?