Canonical Allele Identifier: CA2691711503
Gene: LMX1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.126615364_126615371del , CM000671.2:g.126615364_126615371del GRCh38
NC_000009.11:g.129377643_129377650del , CM000671.1:g.129377643_129377650del GRCh37
NC_000009.10:g.128417464_128417471del NCBI36
NG_017039.1:g.5922_5929del

Transcript Alleles

HGVS Amino-acid change
ENST00000355497.10:c.140-19_140-12del ENSP00000347684.5:n.140-19_140-12del
ENST00000373474.9:c.140-19_140-12del MANE Select ENSP00000362573.3:n.140-19_140-12del
ENST00000526117.6:c.140-19_140-12del ENSP00000436930.1:n.140-19_140-12del
ENST00000355497.9:c.140-19_140-12del ENSP00000347684.5:n.140-19_140-12del
ENST00000373474.8:c.140-19_140-12del ENSP00000362573.3:n.140-19_140-12del
ENST00000526117.5:c.140-19_140-12del ENSP00000436930.1:n.140-19_140-12del
ENST00000561065.1:c.71-19_71-12del ENSP00000453580.1:n.71-19_71-12del
NM_001174146.1:c.140-19_140-12del NP_001167617.1:n.140-19_140-12del
NM_001174147.1:c.140-19_140-12del NP_001167618.1:n.140-19_140-12del
NM_002316.3:c.140-19_140-12del NP_002307.2:n.140-19_140-12del
NM_001174146.2:c.140-19_140-12del NP_001167617.1:n.140-19_140-12del
NM_001174147.2:c.140-19_140-12del MANE Select NP_001167618.1:n.140-19_140-12del
NM_002316.4:c.140-19_140-12del NP_002307.2:n.140-19_140-12del