Canonical Allele Identifier: CA343595698

Gene: LHX4

Linked Data

• gnomAD v4: 1-180266495-A-G
• MyVariant Identifiers: chr1:g.180235630A>G (hg19) ; chr1:g.180266495A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266495A>G , CM000663.2:g.180266495A>G	GRCh38
NC_000001.10:g.180235630A>G , CM000663.1:g.180235630A>G	GRCh37
NC_000001.9:g.178502253A>G	NCBI36
NG_008081.1:g.41189A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.352A>G MANE Select	ENSP00000263726.2:p.Ile118Val
ENST00000263726.3:c.352A>G	ENSP00000263726.2:p.Ile118Val
ENST00000561113.1:c.289A>G
NM_033343.3:c.352A>G	NP_203129.1:p.Ile118Val
XM_011510105.1:c.169A>G	XP_011508407.1:p.Ile57Val
XM_011510106.1:c.169A>G	XP_011508408.1:p.Ile57Val
XM_011510107.1:c.127A>G	XP_011508409.1:p.Ile43Val
XM_011510108.1:c.127A>G	XP_011508410.1:p.Ile43Val
XM_011510105.2:c.169A>G	XP_011508407.1:p.Ile57Val
XM_011510106.3:c.169A>G	XP_011508408.1:p.Ile57Val
XM_011510108.2:c.127A>G	XP_011508410.1:p.Ile43Val
XM_017002755.1:c.127A>G	XP_016858244.1:p.Ile43Val
NM_033343.4:c.352A>G MANE Select	NP_203129.1:p.Ile118Val