Canonical Allele Identifier: CA1008678945

Gene: LMX1A

Linked Data

• dbSNP Id: rs1655309520
• gnomAD v3: 1-165319153-A-AAAATCCAGGAGAAAGACAAGAATGCTCCATATTACCTCTACTATTTAAATACTT
• gnomAD v4: 1-165319153-A-AAAATCCAGGAGAAAGACAAGAATGCTCCATATTACCTCTACTATTTAAATACTT

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165319156_165319209dup , CM000663.2:g.165319156_165319209dup	GRCh38
NC_000001.10:g.165288393_165288446dup , CM000663.1:g.165288393_165288446dup	GRCh37
NC_000001.9:g.163555017_163555070dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294816.6:c.263+33869_263+33922dup	ENSP00000294816.2:n.263+33869_263+33922dup
ENST00000342310.7:c.263+33869_263+33922dup MANE Select	ENSP00000340226.3:n.263+33869_263+33922dup
ENST00000367893.4:c.263+33869_263+33922dup	ENSP00000356868.4:n.263+33869_263+33922dup
NM_001174069.1:c.263+33869_263+33922dup	NP_001167540.1:n.263+33869_263+33922dup
NM_177398.3:c.263+33869_263+33922dup	NP_796372.1:n.263+33869_263+33922dup
XM_011509540.1:c.263+33869_263+33922dup	XP_011507842.1:n.263+33869_263+33922dup
XM_011509540.2:c.263+33869_263+33922dup	XP_011507842.1:n.263+33869_263+33922dup
NM_177398.4:c.263+33869_263+33922dup MANE Select	NP_796372.1:n.263+33869_263+33922dup
NM_001174069.2:c.263+33869_263+33922dup	NP_001167540.1:n.263+33869_263+33922dup