Canonical Allele Identifier: CA526927352

Gene: LMX1A

Linked Data

• dbSNP Id: rs1343394757
• gnomAD v2: 1-165288270-ACACACACACC-A
• gnomAD v3: 1-165319033-ACACACACACC-A
• gnomAD v4: 1-165319033-ACACACACACC-A
• MyVariant Identifiers: chr1:g.165288271_165288280del (hg19) ; chr1:g.165319034_165319043del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165319035_165319044del , CM000663.2:g.165319035_165319044del	GRCh38
NC_000001.10:g.165288272_165288281del , CM000663.1:g.165288272_165288281del	GRCh37
NC_000001.9:g.163554896_163554905del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294816.6:c.263+34033_263+34042del	ENSP00000294816.2:n.263+34033_263+34042del
ENST00000342310.7:c.263+34033_263+34042del MANE Select	ENSP00000340226.3:n.263+34033_263+34042del
ENST00000367893.4:c.263+34033_263+34042del	ENSP00000356868.4:n.263+34033_263+34042del
NM_001174069.1:c.263+34033_263+34042del	NP_001167540.1:n.263+34033_263+34042del
NM_177398.3:c.263+34033_263+34042del	NP_796372.1:n.263+34033_263+34042del
XM_011509540.1:c.263+34033_263+34042del	XP_011507842.1:n.263+34033_263+34042del
XM_011509540.2:c.263+34033_263+34042del	XP_011507842.1:n.263+34033_263+34042del
NM_177398.4:c.263+34033_263+34042del MANE Select	NP_796372.1:n.263+34033_263+34042del
NM_001174069.2:c.263+34033_263+34042del	NP_001167540.1:n.263+34033_263+34042del