Canonical Allele Identifier: CA1879436152
Gene: LMX1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.126615400C= , CM000671.2:g.126615400C= GRCh38
NC_000009.11:g.129377679C= , CM000671.1:g.129377679C= GRCh37
NC_000009.10:g.128417500C= NCBI36
NG_017039.1:g.5958C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355497.10:c.157C= ENSP00000347684.5:p.Pro53=
ENST00000373474.9:c.157C= MANE Select ENSP00000362573.3:p.Pro53=
ENST00000526117.6:c.157C= ENSP00000436930.1:p.Pro53=
ENST00000355497.9:c.157C= ENSP00000347684.5:p.Pro53=
ENST00000373474.8:c.157C= ENSP00000362573.3:p.Pro53=
ENST00000526117.5:c.157C= ENSP00000436930.1:p.Pro53=
ENST00000561065.1:c.88C= ENSP00000453580.1:p.Pro30=
NM_001174146.1:c.157C= NP_001167617.1:p.Pro53=
NM_001174147.1:c.157C= NP_001167618.1:p.Pro53=
NM_002316.3:c.157C= NP_002307.2:p.Pro53=
NM_001174146.2:c.157C= NP_001167617.1:p.Pro53=
NM_001174147.2:c.157C= MANE Select NP_001167618.1:p.Pro53=
NM_002316.4:c.157C= NP_002307.2:p.Pro53=