Canonical Allele Identifier: CA1884109788

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136200700T= , CM000671.2:g.136200700T=	GRCh38
NC_000009.11:g.139092546T= , CM000671.1:g.139092546T=	GRCh37
NC_000009.10:g.138232367T=	NCBI36
NG_008097.1:g.9410A=

Transcript Alleles

HGVS	Amino-acid Change
NM_178138.6:c.133A= MANE Select	NP_835258.1:p.Lys45=
ENST00000371748.10:c.133A= MANE Select	ENSP00000360813.4:p.Lys45=
NM_001363746.1:c.100A=	NP_001350675.1:p.Lys34=
NM_014564.3:c.148A=	NP_055379.1:p.Lys50=
NM_014564.4:c.148A=	NP_055379.1:p.Lys50=
NM_014564.5:c.148A=	NP_055379.1:p.Lys50=
NM_178138.4:c.133A=	NP_835258.1:p.Lys45=
NM_178138.5:c.133A=	NP_835258.1:p.Lys45=
ENST00000371746.7:c.148A=	ENSP00000360811.3:p.Lys50=
ENST00000371746.9:c.148A=	ENSP00000360811.3:p.Lys50=
ENST00000371748.9:c.133A=	ENSP00000360813.4:p.Lys45=
ENST00000619587.1:c.100A=	ENSP00000483080.1:p.Lys34=
ENST00000645419.1:n.257A=
XM_005263410.1:c.100A=	XP_005263467.1:p.Lys34=
XM_017015168.1:c.61A=	XP_016870657.1:p.Lys21=