Canonical Allele Identifier: CA467824641

Gene: LHX3

Linked Data

• MyVariant Identifiers: chr9:g.139089396G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197550G>T , CM000671.2:g.136197550G>T	GRCh38
NC_000009.11:g.139089396G>T , CM000671.1:g.139089396G>T	GRCh37
NC_000009.10:g.138229217G>T	NCBI36
NG_008097.1:g.12560C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.984C>A	ENSP00000360811.3:p.Ala328=
ENST00000371748.10:c.969C>A MANE Select	ENSP00000360813.4:p.Ala323=
ENST00000645419.1:n.1794C>A
ENST00000371746.7:c.984C>A	ENSP00000360811.3:p.Ala328=
ENST00000371748.9:c.969C>A	ENSP00000360813.4:p.Ala323=
ENST00000619587.1:c.936C>A	ENSP00000483080.1:p.Ala312=
NM_014564.3:c.984C>A	NP_055379.1:p.Ala328=
NM_178138.4:c.969C>A	NP_835258.1:p.Ala323=
XM_005263410.1:c.936C>A	XP_005263467.1:p.Ala312=
NM_001363746.1:c.936C>A	NP_001350675.1:p.Ala312=
NM_014564.4:c.984C>A	NP_055379.1:p.Ala328=
NM_178138.5:c.969C>A	NP_835258.1:p.Ala323=
XM_017015168.1:c.897C>A	XP_016870657.1:p.Ala299=
NM_178138.6:c.969C>A MANE Select	NP_835258.1:p.Ala323=
NM_014564.5:c.984C>A	NP_055379.1:p.Ala328=