Canonical Allele Identifier: CA343595826

Gene: LHX4

Linked Data

• MyVariant Identifiers: chr1:g.180235665A>C (hg19) ; chr1:g.180266530A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266530A>C , CM000663.2:g.180266530A>C	GRCh38
NC_000001.10:g.180235665A>C , CM000663.1:g.180235665A>C	GRCh37
NC_000001.9:g.178502288A>C	NCBI36
NG_008081.1:g.41224A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.387A>C MANE Select	ENSP00000263726.2:p.Glu129Asp
ENST00000263726.3:c.387A>C	ENSP00000263726.2:p.Glu129Asp
ENST00000561113.1:c.324A>C
NM_033343.3:c.387A>C	NP_203129.1:p.Glu129Asp
XM_011510105.1:c.204A>C	XP_011508407.1:p.Glu68Asp
XM_011510106.1:c.204A>C	XP_011508408.1:p.Glu68Asp
XM_011510107.1:c.162A>C	XP_011508409.1:p.Glu54Asp
XM_011510108.1:c.162A>C	XP_011508410.1:p.Glu54Asp
XM_011510105.2:c.204A>C	XP_011508407.1:p.Glu68Asp
XM_011510106.3:c.204A>C	XP_011508408.1:p.Glu68Asp
XM_011510108.2:c.162A>C	XP_011508410.1:p.Glu54Asp
XM_017002755.1:c.162A>C	XP_016858244.1:p.Glu54Asp
NM_033343.4:c.387A>C MANE Select	NP_203129.1:p.Glu129Asp