Canonical Allele Identifier: CA375519478

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136198798G>T , CM000671.2:g.136198798G>T	GRCh38
NC_000009.11:g.139090644G>T , CM000671.1:g.139090644G>T	GRCh37
NC_000009.10:g.138230465G>T	NCBI36
NG_008097.1:g.11312C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_178138.6:c.629C>A MANE Select	NP_835258.1:p.Ala210Asp
ENST00000371748.10:c.629C>A MANE Select	ENSP00000360813.4:p.Ala210Asp
NM_001363746.1:c.596C>A	NP_001350675.1:p.Ala199Asp
NM_014564.3:c.644C>A	NP_055379.1:p.Ala215Asp
NM_014564.4:c.644C>A	NP_055379.1:p.Ala215Asp
NM_014564.5:c.644C>A	NP_055379.1:p.Ala215Asp
NM_178138.4:c.629C>A	NP_835258.1:p.Ala210Asp
NM_178138.5:c.629C>A	NP_835258.1:p.Ala210Asp
ENST00000371746.7:c.644C>A	ENSP00000360811.3:p.Ala215Asp
ENST00000371746.9:c.644C>A	ENSP00000360811.3:p.Ala215Asp
ENST00000371748.9:c.629C>A	ENSP00000360813.4:p.Ala210Asp
ENST00000619587.1:c.596C>A	ENSP00000483080.1:p.Ala199Asp
ENST00000645419.1:n.1454C>A
XM_005263410.1:c.596C>A	XP_005263467.1:p.Ala199Asp
XM_017015168.1:c.557C>A	XP_016870657.1:p.Ala186Asp