Canonical Allele Identifier: CA250572

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136198755C>T , CM000671.2:g.136198755C>T	GRCh38
NC_000009.11:g.139090601C>T , CM000671.1:g.139090601C>T	GRCh37
NC_000009.10:g.138230422C>T	NCBI36
NG_008097.1:g.11355G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_178138.6:c.672G>A MANE Select	NP_835258.1:p.Trp224Ter
ENST00000371748.10:c.672G>A MANE Select	ENSP00000360813.4:p.Trp224Ter
NM_001363746.1:c.639G>A	NP_001350675.1:p.Trp213Ter
NM_014564.3:c.687G>A	NP_055379.1:p.Trp229Ter
NM_014564.4:c.687G>A	NP_055379.1:p.Trp229Ter
NM_014564.5:c.687G>A	NP_055379.1:p.Trp229Ter
NM_178138.4:c.672G>A	NP_835258.1:p.Trp224Ter
NM_178138.5:c.672G>A	NP_835258.1:p.Trp224Ter
ENST00000371746.7:c.687G>A	ENSP00000360811.3:p.Trp229Ter
ENST00000371746.9:c.687G>A	ENSP00000360811.3:p.Trp229Ter
ENST00000371748.9:c.672G>A	ENSP00000360813.4:p.Trp224Ter
ENST00000619587.1:c.639G>A	ENSP00000483080.1:p.Trp213Ter
ENST00000645419.1:n.1497G>A
XM_005263410.1:c.639G>A	XP_005263467.1:p.Trp213Ter
XM_017015168.1:c.600G>A	XP_016870657.1:p.Trp200Ter