Canonical Allele Identifier: CA1884103628

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197555C= , CM000671.2:g.136197555C=	GRCh38
NC_000009.11:g.139089401C= , CM000671.1:g.139089401C=	GRCh37
NC_000009.10:g.138229222C=	NCBI36
NG_008097.1:g.12555G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.979G=	ENSP00000360811.3:p.Ala327=
ENST00000371748.10:c.964G= MANE Select	ENSP00000360813.4:p.Ala322=
ENST00000645419.1:n.1789G=
ENST00000371746.7:c.979G=	ENSP00000360811.3:p.Ala327=
ENST00000371748.9:c.964G=	ENSP00000360813.4:p.Ala322=
ENST00000619587.1:c.931G=	ENSP00000483080.1:p.Ala311=
NM_014564.3:c.979G=	NP_055379.1:p.Ala327=
NM_178138.4:c.964G=	NP_835258.1:p.Ala322=
XM_005263410.1:c.931G=	XP_005263467.1:p.Ala311=
NM_001363746.1:c.931G=	NP_001350675.1:p.Ala311=
NM_014564.4:c.979G=	NP_055379.1:p.Ala327=
NM_178138.5:c.964G=	NP_835258.1:p.Ala322=
XM_017015168.1:c.892G=	XP_016870657.1:p.Ala298=
NM_178138.6:c.964G= MANE Select	NP_835258.1:p.Ala322=
NM_014564.5:c.979G=	NP_055379.1:p.Ala327=