Canonical Allele Identifier: CA590568248

Gene: LMX1B

Linked Data

• dbSNP Id: rs1390203407
• gnomAD v2: 9-129377612-G-GGCTGGGCCGGGCGGC
• gnomAD v3: 9-126615333-G-GGCTGGGCCGGGCGGC
• gnomAD v4: 9-126615333-G-GGCTGGGCCGGGCGGC
• MyVariant Identifiers: chr9:g.129377612_129377613insGCTGGGCCGGGCGGC (hg19) ; chr9:g.126615333_126615334insGCTGGGCCGGGCGGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126615338_126615352dup , CM000671.2:g.126615338_126615352dup	GRCh38
NC_000009.11:g.129377617_129377631dup , CM000671.1:g.129377617_129377631dup	GRCh37
NC_000009.10:g.128417438_128417452dup	NCBI36
NG_017039.1:g.5896_5910dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000355497.10:c.140-45_140-31dup	ENSP00000347684.5:n.140-45_140-31dup
ENST00000373474.9:c.140-45_140-31dup MANE Select	ENSP00000362573.3:n.140-45_140-31dup
ENST00000526117.6:c.140-45_140-31dup	ENSP00000436930.1:n.140-45_140-31dup
ENST00000355497.9:c.140-45_140-31dup	ENSP00000347684.5:n.140-45_140-31dup
ENST00000373474.8:c.140-45_140-31dup	ENSP00000362573.3:n.140-45_140-31dup
ENST00000526117.5:c.140-45_140-31dup	ENSP00000436930.1:n.140-45_140-31dup
ENST00000561065.1:c.71-45_71-31dup	ENSP00000453580.1:n.71-45_71-31dup
NM_001174146.1:c.140-45_140-31dup	NP_001167617.1:n.140-45_140-31dup
NM_001174147.1:c.140-45_140-31dup	NP_001167618.1:n.140-45_140-31dup
NM_002316.3:c.140-45_140-31dup	NP_002307.2:n.140-45_140-31dup
NM_001174146.2:c.140-45_140-31dup	NP_001167617.1:n.140-45_140-31dup
NM_001174147.2:c.140-45_140-31dup MANE Select	NP_001167618.1:n.140-45_140-31dup
NM_002316.4:c.140-45_140-31dup	NP_002307.2:n.140-45_140-31dup