Canonical Allele Identifier: CA591365312

Gene: LHX3

Linked Data

• dbSNP Id: rs1351106097
• gnomAD v2: 9-139089391-TGCGGG-T
• MyVariant Identifiers: chr9:g.139089392_139089396del (hg19) ; chr9:g.136197546_136197550del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197550_136197554del , CM000671.2:g.136197550_136197554del	GRCh38
NC_000009.11:g.139089396_139089400del , CM000671.1:g.139089396_139089400del	GRCh37
NC_000009.10:g.138229217_138229221del	NCBI36
NG_008097.1:g.12560_12564del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.984_988del	ENSP00000360811.3:p.Pro329GlufsTer?
ENST00000371748.10:c.969_973del MANE Select	ENSP00000360813.4:p.Pro324GlufsTer?
ENST00000645419.1:n.1794_1798del
ENST00000371746.7:c.984_988del	ENSP00000360811.3:p.Pro329GlufsTer?
ENST00000371748.9:c.969_973del	ENSP00000360813.4:p.Pro324GlufsTer?
ENST00000619587.1:c.936_940del	ENSP00000483080.1:p.Pro313GlufsTer?
NM_014564.3:c.984_988del	NP_055379.1:p.Pro329GlufsTer?
NM_178138.4:c.969_973del	NP_835258.1:p.Pro324GlufsTer?
XM_005263410.1:c.936_940del	XP_005263467.1:p.Pro313GlufsTer?
NM_001363746.1:c.936_940del	NP_001350675.1:p.Pro313GlufsTer?
NM_014564.4:c.984_988del	NP_055379.1:p.Pro329GlufsTer?
NM_178138.5:c.969_973del	NP_835258.1:p.Pro324GlufsTer?
XM_017015168.1:c.897_901del	XP_016870657.1:p.Pro300GlufsTer?
NM_178138.6:c.969_973del MANE Select	NP_835258.1:p.Pro324GlufsTer?
NM_014564.5:c.984_988del	NP_055379.1:p.Pro329GlufsTer?