Canonical Allele Identifier: CA5330602

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136200740G>A , CM000671.2:g.136200740G>A	GRCh38
NC_000009.11:g.139092586G>A , CM000671.1:g.139092586G>A	GRCh37
NC_000009.10:g.138232407G>A	NCBI36
NG_008097.1:g.9370C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_178138.6:c.93C>T MANE Select	NP_835258.1:p.Cys31=
ENST00000371748.10:c.93C>T MANE Select	ENSP00000360813.4:p.Cys31=
NM_001363746.1:c.60C>T	NP_001350675.1:p.Cys20=
NM_014564.3:c.108C>T	NP_055379.1:p.Cys36=
NM_014564.4:c.108C>T	NP_055379.1:p.Cys36=
NM_014564.5:c.108C>T	NP_055379.1:p.Cys36=
NM_178138.4:c.93C>T	NP_835258.1:p.Cys31=
NM_178138.5:c.93C>T	NP_835258.1:p.Cys31=
ENST00000371746.7:c.108C>T	ENSP00000360811.3:p.Cys36=
ENST00000371746.9:c.108C>T	ENSP00000360811.3:p.Cys36=
ENST00000371748.9:c.93C>T	ENSP00000360813.4:p.Cys31=
ENST00000619587.1:c.60C>T	ENSP00000483080.1:p.Cys20=
ENST00000645419.1:n.217C>T
XM_005263410.1:c.60C>T	XP_005263467.1:p.Cys20=
XM_017015168.1:c.21C>T	XP_016870657.1:p.Cys7=