Canonical Allele Identifier: CA467824647

Gene: LHX3

Linked Data

• MyVariant Identifiers: chr9:g.139089399G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197553G>C , CM000671.2:g.136197553G>C	GRCh38
NC_000009.11:g.139089399G>C , CM000671.1:g.139089399G>C	GRCh37
NC_000009.10:g.138229220G>C	NCBI36
NG_008097.1:g.12557C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.981C>G	ENSP00000360811.3:p.Ala327=
ENST00000371748.10:c.966C>G MANE Select	ENSP00000360813.4:p.Ala322=
ENST00000645419.1:n.1791C>G
ENST00000371746.7:c.981C>G	ENSP00000360811.3:p.Ala327=
ENST00000371748.9:c.966C>G	ENSP00000360813.4:p.Ala322=
ENST00000619587.1:c.933C>G	ENSP00000483080.1:p.Ala311=
NM_014564.3:c.981C>G	NP_055379.1:p.Ala327=
NM_178138.4:c.966C>G	NP_835258.1:p.Ala322=
XM_005263410.1:c.933C>G	XP_005263467.1:p.Ala311=
NM_001363746.1:c.933C>G	NP_001350675.1:p.Ala311=
NM_014564.4:c.981C>G	NP_055379.1:p.Ala327=
NM_178138.5:c.966C>G	NP_835258.1:p.Ala322=
XM_017015168.1:c.894C>G	XP_016870657.1:p.Ala298=
NM_178138.6:c.966C>G MANE Select	NP_835258.1:p.Ala322=
NM_014564.5:c.981C>G	NP_055379.1:p.Ala327=