Canonical Allele Identifier: CA422047539

Gene: LHX4

Linked Data

• gnomAD v4: 1-180266512-G-A
• MyVariant Identifiers: chr1:g.180235647G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266512G>A , CM000663.2:g.180266512G>A	GRCh38
NC_000001.10:g.180235647G>A , CM000663.1:g.180235647G>A	GRCh37
NC_000001.9:g.178502270G>A	NCBI36
NG_008081.1:g.41206G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.369G>A MANE Select	ENSP00000263726.2:p.Gln123=
ENST00000263726.3:c.369G>A	ENSP00000263726.2:p.Gln123=
ENST00000561113.1:c.306G>A
NM_033343.3:c.369G>A	NP_203129.1:p.Gln123=
XM_011510105.1:c.186G>A	XP_011508407.1:p.Gln62=
XM_011510106.1:c.186G>A	XP_011508408.1:p.Gln62=
XM_011510107.1:c.144G>A	XP_011508409.1:p.Gln48=
XM_011510108.1:c.144G>A	XP_011508410.1:p.Gln48=
XM_011510105.2:c.186G>A	XP_011508407.1:p.Gln62=
XM_011510106.3:c.186G>A	XP_011508408.1:p.Gln62=
XM_011510108.2:c.144G>A	XP_011508410.1:p.Gln48=
XM_017002755.1:c.144G>A	XP_016858244.1:p.Gln48=
NM_033343.4:c.369G>A MANE Select	NP_203129.1:p.Gln123=