Canonical Allele Identifier: CA343595713

Gene: LHX4

Linked Data

• MyVariant Identifiers: chr1:g.180235634T>A (hg19) ; chr1:g.180266499T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266499T>A , CM000663.2:g.180266499T>A	GRCh38
NC_000001.10:g.180235634T>A , CM000663.1:g.180235634T>A	GRCh37
NC_000001.9:g.178502257T>A	NCBI36
NG_008081.1:g.41193T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.356T>A MANE Select	ENSP00000263726.2:p.Ile119Asn
ENST00000263726.3:c.356T>A	ENSP00000263726.2:p.Ile119Asn
ENST00000561113.1:c.293T>A
NM_033343.3:c.356T>A	NP_203129.1:p.Ile119Asn
XM_011510105.1:c.173T>A	XP_011508407.1:p.Ile58Asn
XM_011510106.1:c.173T>A	XP_011508408.1:p.Ile58Asn
XM_011510107.1:c.131T>A	XP_011508409.1:p.Ile44Asn
XM_011510108.1:c.131T>A	XP_011508410.1:p.Ile44Asn
XM_011510105.2:c.173T>A	XP_011508407.1:p.Ile58Asn
XM_011510106.3:c.173T>A	XP_011508408.1:p.Ile58Asn
XM_011510108.2:c.131T>A	XP_011508410.1:p.Ile44Asn
XM_017002755.1:c.131T>A	XP_016858244.1:p.Ile44Asn
NM_033343.4:c.356T>A MANE Select	NP_203129.1:p.Ile119Asn