Canonical Allele Identifier: CA467712560

Gene: LHX3

Linked Data

• MyVariant Identifiers: chr9:g.139089504C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197658C>A , CM000671.2:g.136197658C>A	GRCh38
NC_000009.11:g.139089504C>A , CM000671.1:g.139089504C>A	GRCh37
NC_000009.10:g.138229325C>A	NCBI36
NG_008097.1:g.12452G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.876G>T	ENSP00000360811.3:p.Ser292=
ENST00000371748.10:c.861G>T MANE Select	ENSP00000360813.4:p.Ser287=
ENST00000645419.1:n.1686G>T
ENST00000371746.7:c.876G>T	ENSP00000360811.3:p.Ser292=
ENST00000371748.9:c.861G>T	ENSP00000360813.4:p.Ser287=
ENST00000619587.1:c.828G>T	ENSP00000483080.1:p.Ser276=
NM_014564.3:c.876G>T	NP_055379.1:p.Ser292=
NM_178138.4:c.861G>T	NP_835258.1:p.Ser287=
XM_005263410.1:c.828G>T	XP_005263467.1:p.Ser276=
NM_001363746.1:c.828G>T	NP_001350675.1:p.Ser276=
NM_014564.4:c.876G>T	NP_055379.1:p.Ser292=
NM_178138.5:c.861G>T	NP_835258.1:p.Ser287=
XM_017015168.1:c.789G>T	XP_016870657.1:p.Ser263=
NM_178138.6:c.861G>T MANE Select	NP_835258.1:p.Ser287=
NM_014564.5:c.876G>T	NP_055379.1:p.Ser292=