Canonical Allele Identifier: CA1879436197

Gene: LMX1B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.126615527_126615532delinsACTTCC , CM000671.2:g.126615527_126615532delinsACTTCC	GRCh38
NC_000009.11:g.129377806_129377811delinsACTTCC , CM000671.1:g.129377806_129377811delinsACTTCC	GRCh37
NC_000009.10:g.128417627_128417632delinsACTTCC	NCBI36
NG_017039.1:g.6085_6090delinsACTTCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000355497.10:c.284_289delinsACTTCC	ENSP00000347684.5:p.Tyr95=
ENST00000373474.9:c.284_289delinsACTTCC MANE Select	ENSP00000362573.3:p.Tyr95=
ENST00000526117.6:c.284_289delinsACTTCC	ENSP00000436930.1:p.Tyr95=
ENST00000355497.9:c.284_289delinsACTTCC	ENSP00000347684.5:p.Tyr95=
ENST00000373474.8:c.284_289delinsACTTCC	ENSP00000362573.3:p.Tyr95=
ENST00000526117.5:c.284_289delinsACTTCC	ENSP00000436930.1:p.Tyr95=
ENST00000561065.1:c.215_220delinsACTTCC	ENSP00000453580.1:p.Tyr72=
NM_001174146.1:c.284_289delinsACTTCC	NP_001167617.1:p.Tyr95=
NM_001174147.1:c.284_289delinsACTTCC	NP_001167618.1:p.Tyr95=
NM_002316.3:c.284_289delinsACTTCC	NP_002307.2:p.Tyr95=
NM_001174146.2:c.284_289delinsACTTCC	NP_001167617.1:p.Tyr95=
NM_001174147.2:c.284_289delinsACTTCC MANE Select	NP_001167618.1:p.Tyr95=
NM_002316.4:c.284_289delinsACTTCC	NP_002307.2:p.Tyr95=