Canonical Allele Identifier: CA3165530932

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136200737A= , CM000671.2:g.136200737A=	GRCh38
NC_000009.11:g.139092583A= , CM000671.1:g.139092583A=	GRCh37
NC_000009.10:g.138232404A=	NCBI36
NG_008097.1:g.9373T=

Transcript Alleles

HGVS	Amino-acid Change
NM_178138.6:c.96T= MANE Select	NP_835258.1:p.Ala32=
ENST00000371748.10:c.96T= MANE Select	ENSP00000360813.4:p.Ala32=
NM_001363746.1:c.63T=	NP_001350675.1:p.Ala21=
NM_014564.3:c.111T=	NP_055379.1:p.Ala37=
NM_014564.4:c.111T=	NP_055379.1:p.Ala37=
NM_014564.5:c.111T=	NP_055379.1:p.Ala37=
NM_178138.4:c.96T=	NP_835258.1:p.Ala32=
NM_178138.5:c.96T=	NP_835258.1:p.Ala32=
ENST00000371746.7:c.111T=	ENSP00000360811.3:p.Ala37=
ENST00000371746.9:c.111T=	ENSP00000360811.3:p.Ala37=
ENST00000371748.9:c.96T=	ENSP00000360813.4:p.Ala32=
ENST00000619587.1:c.63T=	ENSP00000483080.1:p.Ala21=
ENST00000645419.1:n.220T=
XM_005263410.1:c.63T=	XP_005263467.1:p.Ala21=
XM_017015168.1:c.24T=	XP_016870657.1:p.Ala8=