Canonical Allele Identifier: CA2695211429
Gene: LMX1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.126693254dup , CM000671.2:g.126693254dup GRCh38
NC_000009.11:g.129455533dup , CM000671.1:g.129455533dup GRCh37
NC_000009.10:g.128495354dup NCBI36
NG_017039.1:g.83812dup

Transcript Alleles

HGVS Amino-acid change
ENST00000355497.10:c.672dup ENSP00000347684.5:p.Ile225HisfsTer?
ENST00000373474.9:c.672dup MANE Select ENSP00000362573.3:p.Ile225HisfsTer?
ENST00000526117.6:c.672dup ENSP00000436930.1:p.Ile225HisfsTer?
ENST00000355497.9:c.672dup ENSP00000347684.5:p.Ile225HisfsTer?
ENST00000373474.8:c.672dup ENSP00000362573.3:p.Ile225HisfsTer?
ENST00000526117.5:c.672dup ENSP00000436930.1:p.Ile225HisfsTer?
ENST00000561065.1:c.603dup ENSP00000453580.1:p.Ile202HisfsTer?
NM_001174146.1:c.672dup NP_001167617.1:p.Ile225HisfsTer?
NM_001174147.1:c.672dup NP_001167618.1:p.Ile225HisfsTer?
NM_002316.3:c.672dup NP_002307.2:p.Ile225HisfsTer?
NM_001174146.2:c.672dup NP_001167617.1:p.Ile225HisfsTer?
NM_001174147.2:c.672dup MANE Select NP_001167618.1:p.Ile225HisfsTer?
NM_002316.4:c.672dup NP_002307.2:p.Ile225HisfsTer?