Canonical Allele Identifier: CA5330601

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136200739C>T , CM000671.2:g.136200739C>T	GRCh38
NC_000009.11:g.139092585C>T , CM000671.1:g.139092585C>T	GRCh37
NC_000009.10:g.138232406C>T	NCBI36
NG_008097.1:g.9371G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371746.9:c.109G>A	ENSP00000360811.3:p.Ala37Thr
ENST00000371748.10:c.94G>A MANE Select	ENSP00000360813.4:p.Ala32Thr
ENST00000645419.1:n.218G>A
ENST00000371746.7:c.109G>A	ENSP00000360811.3:p.Ala37Thr
ENST00000371748.9:c.94G>A	ENSP00000360813.4:p.Ala32Thr
ENST00000619587.1:c.61G>A	ENSP00000483080.1:p.Ala21Thr
NM_014564.3:c.109G>A	NP_055379.1:p.Ala37Thr
NM_178138.4:c.94G>A	NP_835258.1:p.Ala32Thr
XM_005263410.1:c.61G>A	XP_005263467.1:p.Ala21Thr
NM_001363746.1:c.61G>A	NP_001350675.1:p.Ala21Thr
NM_014564.4:c.109G>A	NP_055379.1:p.Ala37Thr
NM_178138.5:c.94G>A	NP_835258.1:p.Ala32Thr
XM_017015168.1:c.22G>A	XP_016870657.1:p.Ala8Thr
NM_178138.6:c.94G>A MANE Select	NP_835258.1:p.Ala32Thr
NM_014564.5:c.109G>A	NP_055379.1:p.Ala37Thr