Canonical Allele Identifier: CA1204368302

Gene: LMX1A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165319029_165319043delinsACACACACACACACC , CM000663.2:g.165319029_165319043delinsACACACACACACACC	GRCh38
NC_000001.10:g.165288266_165288280delinsACACACACACACACC , CM000663.1:g.165288266_165288280delinsACACACACACACACC	GRCh37
NC_000001.9:g.163554890_163554904delinsACACACACACACACC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294816.6:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT	ENSP00000294816.2:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
ENST00000342310.7:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT MANE Select	ENSP00000340226.3:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
ENST00000367893.4:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT	ENSP00000356868.4:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
NM_001174069.1:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT	NP_001167540.1:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
NM_177398.3:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT	NP_796372.1:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
XM_011509540.1:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT	XP_011507842.1:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
XM_011509540.2:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT	XP_011507842.1:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
NM_177398.4:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT MANE Select	NP_796372.1:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT
NM_001174069.2:c.263+34033_263+34047delinsGGTGTGTGTGTGTGT	NP_001167540.1:n.263+34033_263+34047delinsGGTGTGTGTGTGTGT