Canonical Allele Identifier: CA375518372

Gene: LHX3

Linked Data

• gnomAD v4: 9-136197349-A-C
• MyVariant Identifiers: chr9:g.139089195A>C (hg19) ; chr9:g.136197349A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197349A>C , CM000671.2:g.136197349A>C	GRCh38
NC_000009.11:g.139089195A>C , CM000671.1:g.139089195A>C	GRCh37
NC_000009.10:g.138229016A>C	NCBI36
NG_008097.1:g.12761T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371746.9:c.1185T>G	ENSP00000360811.3:p.Asp395Glu
ENST00000371748.10:c.1170T>G MANE Select	ENSP00000360813.4:p.Asp390Glu
ENST00000645419.1:n.1995T>G
ENST00000371746.7:c.1185T>G	ENSP00000360811.3:p.Asp395Glu
ENST00000371748.9:c.1170T>G	ENSP00000360813.4:p.Asp390Glu
ENST00000619587.1:c.1137T>G	ENSP00000483080.1:p.Asp379Glu
NM_014564.3:c.1185T>G	NP_055379.1:p.Asp395Glu
NM_178138.4:c.1170T>G	NP_835258.1:p.Asp390Glu
XM_005263410.1:c.1137T>G	XP_005263467.1:p.Asp379Glu
NM_001363746.1:c.1137T>G	NP_001350675.1:p.Asp379Glu
NM_014564.4:c.1185T>G	NP_055379.1:p.Asp395Glu
NM_178138.5:c.1170T>G	NP_835258.1:p.Asp390Glu
XM_017015168.1:c.1098T>G	XP_016870657.1:p.Asp366Glu
NM_178138.6:c.1170T>G MANE Select	NP_835258.1:p.Asp390Glu
NM_014564.5:c.1185T>G	NP_055379.1:p.Asp395Glu