Canonical Allele Identifier: CA1210607169

Gene: LHX4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.180266460A= , CM000663.2:g.180266460A=	GRCh38
NC_000001.10:g.180235595A= , CM000663.1:g.180235595A=	GRCh37
NC_000001.9:g.178502218A=	NCBI36
NG_008081.1:g.41154A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263726.4:c.317A= MANE Select	ENSP00000263726.2:p.Gln106=
ENST00000263726.3:c.317A=	ENSP00000263726.2:p.Gln106=
ENST00000561113.1:c.254A=
NM_033343.3:c.317A=	NP_203129.1:p.Gln106=
XM_011510105.1:c.134A=	XP_011508407.1:p.Gln45=
XM_011510106.1:c.134A=	XP_011508408.1:p.Gln45=
XM_011510107.1:c.92A=	XP_011508409.1:p.Gln31=
XM_011510108.1:c.92A=	XP_011508410.1:p.Gln31=
XM_011510105.2:c.134A=	XP_011508407.1:p.Gln45=
XM_011510106.3:c.134A=	XP_011508408.1:p.Gln45=
XM_011510108.2:c.92A=	XP_011508410.1:p.Gln31=
XM_017002755.1:c.92A=	XP_016858244.1:p.Gln31=
NM_033343.4:c.317A= MANE Select	NP_203129.1:p.Gln106=