Canonical Allele Identifier: CA467712563

Gene: LHX3

Linked Data

• gnomAD v4: 9-136197661-G-A
• MyVariant Identifiers: chr9:g.139089507G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136197661G>A , CM000671.2:g.136197661G>A	GRCh38
NC_000009.11:g.139089507G>A , CM000671.1:g.139089507G>A	GRCh37
NC_000009.10:g.138229328G>A	NCBI36
NG_008097.1:g.12449C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000371746.9:c.873C>T	ENSP00000360811.3:p.Pro291=
ENST00000371748.10:c.858C>T MANE Select	ENSP00000360813.4:p.Pro286=
ENST00000645419.1:n.1683C>T
ENST00000371746.7:c.873C>T	ENSP00000360811.3:p.Pro291=
ENST00000371748.9:c.858C>T	ENSP00000360813.4:p.Pro286=
ENST00000619587.1:c.825C>T	ENSP00000483080.1:p.Pro275=
NM_014564.3:c.873C>T	NP_055379.1:p.Pro291=
NM_178138.4:c.858C>T	NP_835258.1:p.Pro286=
XM_005263410.1:c.825C>T	XP_005263467.1:p.Pro275=
NM_001363746.1:c.825C>T	NP_001350675.1:p.Pro275=
NM_014564.4:c.873C>T	NP_055379.1:p.Pro291=
NM_178138.5:c.858C>T	NP_835258.1:p.Pro286=
XM_017015168.1:c.786C>T	XP_016870657.1:p.Pro262=
NM_178138.6:c.858C>T MANE Select	NP_835258.1:p.Pro286=
NM_014564.5:c.873C>T	NP_055379.1:p.Pro291=