Canonical Allele Identifier: CA374910054

Gene: LMX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126615480G>T , CM000671.2:g.126615480G>T	GRCh38
NC_000009.11:g.129377759G>T , CM000671.1:g.129377759G>T	GRCh37
NC_000009.10:g.128417580G>T	NCBI36
NG_017039.1:g.6038G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001174147.2:c.237G>T MANE Select	NP_001167618.1:p.Glu79Asp
ENST00000373474.9:c.237G>T MANE Select	ENSP00000362573.3:p.Glu79Asp
NM_001174146.1:c.237G>T	NP_001167617.1:p.Glu79Asp
NM_001174146.2:c.237G>T	NP_001167617.1:p.Glu79Asp
NM_001174147.1:c.237G>T	NP_001167618.1:p.Glu79Asp
NM_002316.3:c.237G>T	NP_002307.2:p.Glu79Asp
NM_002316.4:c.237G>T	NP_002307.2:p.Glu79Asp
ENST00000355497.10:c.237G>T	ENSP00000347684.5:p.Glu79Asp
ENST00000355497.9:c.237G>T	ENSP00000347684.5:p.Glu79Asp
ENST00000373474.8:c.237G>T	ENSP00000362573.3:p.Glu79Asp
ENST00000526117.5:c.237G>T	ENSP00000436930.1:p.Glu79Asp
ENST00000526117.6:c.237G>T	ENSP00000436930.1:p.Glu79Asp
ENST00000561065.1:c.168G>T	ENSP00000453580.1:p.Glu56Asp