Canonical Allele Identifier: CA890570045
Gene: LMX1A HGNC NCBI

Linked Data

dbSNP Id: rs35582531

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165319031_165319042del , CM000663.2:g.165319031_165319042del GRCh38
NC_000001.10:g.165288268_165288279del , CM000663.1:g.165288268_165288279del GRCh37
NC_000001.9:g.163554892_163554903del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000294816.6:c.263+34065_263+34076del ENSP00000294816.2:n.263+34065_263+34076de...
ENST00000342310.7:c.263+34065_263+34076del MANE Select ENSP00000340226.3:n.263+34065_263+34076de...
ENST00000367893.4:c.263+34065_263+34076del ENSP00000356868.4:n.263+34065_263+34076de...
NM_001174069.1:c.263+34065_263+34076del NP_001167540.1:n.263+34065_263+34076del
NM_177398.3:c.263+34065_263+34076del NP_796372.1:n.263+34065_263+34076del
XM_011509540.1:c.263+34065_263+34076del XP_011507842.1:n.263+34065_263+34076del
XM_011509540.2:c.263+34065_263+34076del XP_011507842.1:n.263+34065_263+34076del
NM_177398.4:c.263+34065_263+34076del MANE Select NP_796372.1:n.263+34065_263+34076del
NM_001174069.2:c.263+34065_263+34076del NP_001167540.1:n.263+34065_263+34076del