Canonical Allele Identifier: CA467712556

Gene: LHX3

Linked Data

• gnomAD v4: 9-136197652-G-T
• MyVariant Identifiers: chr9:g.139089498G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197652G>T , CM000671.2:g.136197652G>T	GRCh38
NC_000009.11:g.139089498G>T , CM000671.1:g.139089498G>T	GRCh37
NC_000009.10:g.138229319G>T	NCBI36
NG_008097.1:g.12458C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.882C>A	ENSP00000360811.3:p.Ala294=
ENST00000371748.10:c.867C>A MANE Select	ENSP00000360813.4:p.Ala289=
ENST00000645419.1:n.1692C>A
ENST00000371746.7:c.882C>A	ENSP00000360811.3:p.Ala294=
ENST00000371748.9:c.867C>A	ENSP00000360813.4:p.Ala289=
ENST00000619587.1:c.834C>A	ENSP00000483080.1:p.Ala278=
NM_014564.3:c.882C>A	NP_055379.1:p.Ala294=
NM_178138.4:c.867C>A	NP_835258.1:p.Ala289=
XM_005263410.1:c.834C>A	XP_005263467.1:p.Ala278=
NM_001363746.1:c.834C>A	NP_001350675.1:p.Ala278=
NM_014564.4:c.882C>A	NP_055379.1:p.Ala294=
NM_178138.5:c.867C>A	NP_835258.1:p.Ala289=
XM_017015168.1:c.795C>A	XP_016870657.1:p.Ala265=
NM_178138.6:c.867C>A MANE Select	NP_835258.1:p.Ala289=
NM_014564.5:c.882C>A	NP_055379.1:p.Ala294=