Canonical Allele Identifier: CA2573131281

Gene: LHX4

Linked Data

• ClinVar Variation Id: 1428279
• ClinVar RCV Id: RCV001936225
• dbSNP Id: rs2149263256

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266525del , CM000663.2:g.180266525del	GRCh38
NC_000001.10:g.180235660del , CM000663.1:g.180235660del	GRCh37
NC_000001.9:g.178502283del	NCBI36
NG_008081.1:g.41219del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.382del MANE Select	ENSP00000263726.2:p.Asp128ThrfsTer?
ENST00000263726.3:c.382del	ENSP00000263726.2:p.Asp128ThrfsTer?
ENST00000561113.1:c.319del
NM_033343.3:c.382del	NP_203129.1:p.Asp128ThrfsTer?
XM_011510105.1:c.199del	XP_011508407.1:p.Asp67ThrfsTer?
XM_011510106.1:c.199del	XP_011508408.1:p.Asp67ThrfsTer?
XM_011510107.1:c.157del	XP_011508409.1:p.Asp53ThrfsTer?
XM_011510108.1:c.157del	XP_011508410.1:p.Asp53ThrfsTer?
XM_011510105.2:c.199del	XP_011508407.1:p.Asp67ThrfsTer?
XM_011510106.3:c.199del	XP_011508408.1:p.Asp67ThrfsTer?
XM_011510108.2:c.157del	XP_011508410.1:p.Asp53ThrfsTer?
XM_017002755.1:c.157del	XP_016858244.1:p.Asp53ThrfsTer?
NM_033343.4:c.382del MANE Select	NP_203129.1:p.Asp128ThrfsTer?