Canonical Allele Identifier: CA1139661344

Gene: LHX3

Linked Data

• ClinVar Variation Id: 914719
• ClinVar RCV Id: RCV001169028
• dbSNP Id: rs1831495899

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136196633G>A , CM000671.2:g.136196633G>A	GRCh38
NC_000009.11:g.139088479G>A , CM000671.1:g.139088479G>A	GRCh37
NC_000009.10:g.138228300G>A	NCBI36
NG_008097.1:g.13477C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371746.9:c.*692C>T	ENSP00000360811.3:n.*692C>T
ENST00000371748.10:c.*692C>T MANE Select	ENSP00000360813.4:n.*692C>T
ENST00000645419.1:n.2711C>T
ENST00000371746.7:c.*692C>T	ENSP00000360811.3:n.*692C>T
ENST00000371748.9:c.*692C>T	ENSP00000360813.4:n.*692C>T
ENST00000619587.1:c.*692C>T	ENSP00000483080.1:n.*692C>T
NM_014564.3:c.*692C>T	NP_055379.1:n.*692C>T
NM_178138.4:c.*692C>T	NP_835258.1:n.*692C>T
XM_005263410.1:c.*692C>T	XP_005263467.1:n.*692C>T
NM_001363746.1:c.*692C>T	NP_001350675.1:n.*692C>T
NM_014564.4:c.*692C>T	NP_055379.1:n.*692C>T
NM_178138.5:c.*692C>T	NP_835258.1:n.*692C>T
XM_017015168.1:c.1814C>T	XP_016870657.1:n.1814C>T
NM_178138.6:c.*692C>T MANE Select	NP_835258.1:n.*692C>T
NM_014564.5:c.*692C>T	NP_055379.1:n.*692C>T