Canonical Allele Identifier: CA1884103602

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197551G= , CM000671.2:g.136197551G=	GRCh38
NC_000009.11:g.139089397G= , CM000671.1:g.139089397G=	GRCh37
NC_000009.10:g.138229218G=	NCBI36
NG_008097.1:g.12559C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.983C=	ENSP00000360811.3:p.Ala328=
ENST00000371748.10:c.968C= MANE Select	ENSP00000360813.4:p.Ala323=
ENST00000645419.1:n.1793C=
ENST00000371746.7:c.983C=	ENSP00000360811.3:p.Ala328=
ENST00000371748.9:c.968C=	ENSP00000360813.4:p.Ala323=
ENST00000619587.1:c.935C=	ENSP00000483080.1:p.Ala312=
NM_014564.3:c.983C=	NP_055379.1:p.Ala328=
NM_178138.4:c.968C=	NP_835258.1:p.Ala323=
XM_005263410.1:c.935C=	XP_005263467.1:p.Ala312=
NM_001363746.1:c.935C=	NP_001350675.1:p.Ala312=
NM_014564.4:c.983C=	NP_055379.1:p.Ala328=
NM_178138.5:c.968C=	NP_835258.1:p.Ala323=
XM_017015168.1:c.896C=	XP_016870657.1:p.Ala299=
NM_178138.6:c.968C= MANE Select	NP_835258.1:p.Ala323=
NM_014564.5:c.983C=	NP_055379.1:p.Ala328=