Canonical Allele Identifier: CA422047531

Gene: LHX4

Linked Data

• MyVariant Identifiers: chr1:g.180235635C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266500C>A , CM000663.2:g.180266500C>A	GRCh38
NC_000001.10:g.180235635C>A , CM000663.1:g.180235635C>A	GRCh37
NC_000001.9:g.178502258C>A	NCBI36
NG_008081.1:g.41194C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.357C>A MANE Select	ENSP00000263726.2:p.Ile119=
ENST00000263726.3:c.357C>A	ENSP00000263726.2:p.Ile119=
ENST00000561113.1:c.294C>A
NM_033343.3:c.357C>A	NP_203129.1:p.Ile119=
XM_011510105.1:c.174C>A	XP_011508407.1:p.Ile58=
XM_011510106.1:c.174C>A	XP_011508408.1:p.Ile58=
XM_011510107.1:c.132C>A	XP_011508409.1:p.Ile44=
XM_011510108.1:c.132C>A	XP_011508410.1:p.Ile44=
XM_011510105.2:c.174C>A	XP_011508407.1:p.Ile58=
XM_011510106.3:c.174C>A	XP_011508408.1:p.Ile58=
XM_011510108.2:c.132C>A	XP_011508410.1:p.Ile44=
XM_017002755.1:c.132C>A	XP_016858244.1:p.Ile44=
NM_033343.4:c.357C>A MANE Select	NP_203129.1:p.Ile119=