Canonical Allele Identifier: CA1884108163

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136199800T= , CM000671.2:g.136199800T=	GRCh38
NC_000009.11:g.139091646T= , CM000671.1:g.139091646T=	GRCh37
NC_000009.10:g.138231467T=	NCBI36
NG_008097.1:g.10310A=

Transcript Alleles

HGVS	Amino-acid Change
NM_178138.6:c.332A= MANE Select	NP_835258.1:p.Tyr111=
ENST00000371748.10:c.332A= MANE Select	ENSP00000360813.4:p.Tyr111=
NM_001363746.1:c.299A=	NP_001350675.1:p.Tyr100=
NM_014564.3:c.347A=	NP_055379.1:p.Tyr116=
NM_014564.4:c.347A=	NP_055379.1:p.Tyr116=
NM_014564.5:c.347A=	NP_055379.1:p.Tyr116=
NM_178138.4:c.332A=	NP_835258.1:p.Tyr111=
NM_178138.5:c.332A=	NP_835258.1:p.Tyr111=
ENST00000371746.7:c.347A=	ENSP00000360811.3:p.Tyr116=
ENST00000371746.9:c.347A=	ENSP00000360811.3:p.Tyr116=
ENST00000371748.9:c.332A=	ENSP00000360813.4:p.Tyr111=
ENST00000619587.1:c.299A=	ENSP00000483080.1:p.Tyr100=
ENST00000645419.1:n.1157A=
XM_005263410.1:c.299A=	XP_005263467.1:p.Tyr100=
XM_017015168.1:c.260A=	XP_016870657.1:p.Tyr87=