Canonical Allele Identifier: CA250569

Gene: LHX3

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136200737del , CM000671.2:g.136200737del	GRCh38
NC_000009.11:g.139092583del , CM000671.1:g.139092583del	GRCh37
NC_000009.10:g.138232404del	NCBI36
NG_008097.1:g.9373del

Transcript Alleles

HGVS	Amino-acid Change
NM_178138.6:c.96del MANE Select	NP_835258.1:p.Gly33AlafsTer?
ENST00000371748.10:c.96del MANE Select	ENSP00000360813.4:p.Gly33AlafsTer?
NM_001363746.1:c.63del	NP_001350675.1:p.Gly22AlafsTer?
NM_014564.3:c.111del	NP_055379.1:p.Gly38AlafsTer?
NM_014564.4:c.111del	NP_055379.1:p.Gly38AlafsTer?
NM_014564.5:c.111del	NP_055379.1:p.Gly38AlafsTer?
NM_178138.4:c.96del	NP_835258.1:p.Gly33AlafsTer?
NM_178138.5:c.96del	NP_835258.1:p.Gly33AlafsTer?
ENST00000371746.7:c.111del	ENSP00000360811.3:p.Gly38AlafsTer?
ENST00000371746.9:c.111del	ENSP00000360811.3:p.Gly38AlafsTer?
ENST00000371748.9:c.96del	ENSP00000360813.4:p.Gly33AlafsTer?
ENST00000619587.1:c.63del	ENSP00000483080.1:p.Gly22AlafsTer?
ENST00000645419.1:n.220del
XM_005263410.1:c.63del	XP_005263467.1:p.Gly22AlafsTer?
XM_017015168.1:c.24del	XP_016870657.1:p.Gly9AlafsTer?