Canonical Allele Identifier: CA1879478523

Gene: LMX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126693245_126693246delinsAC , CM000671.2:g.126693245_126693246delinsAC	GRCh38
NC_000009.11:g.129455524_129455525delinsAC , CM000671.1:g.129455524_129455525delinsAC	GRCh37
NC_000009.10:g.128495345_128495346delinsAC	NCBI36
NG_017039.1:g.83803_83804delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000355497.10:c.663_664delinsAC	ENSP00000347684.5:p.Arg221=
ENST00000373474.9:c.663_664delinsAC MANE Select	ENSP00000362573.3:p.Arg221=
ENST00000526117.6:c.663_664delinsAC	ENSP00000436930.1:p.Arg221=
ENST00000355497.9:c.663_664delinsAC	ENSP00000347684.5:p.Arg221=
ENST00000373474.8:c.663_664delinsAC	ENSP00000362573.3:p.Arg221=
ENST00000526117.5:c.663_664delinsAC	ENSP00000436930.1:p.Arg221=
ENST00000561065.1:c.594_595delinsAC	ENSP00000453580.1:p.Arg198=
NM_001174146.1:c.663_664delinsAC	NP_001167617.1:p.Arg221=
NM_001174147.1:c.663_664delinsAC	NP_001167618.1:p.Arg221=
NM_002316.3:c.663_664delinsAC	NP_002307.2:p.Arg221=
NM_001174146.2:c.663_664delinsAC	NP_001167617.1:p.Arg221=
NM_001174147.2:c.663_664delinsAC MANE Select	NP_001167618.1:p.Arg221=
NM_002316.4:c.663_664delinsAC	NP_002307.2:p.Arg221=