Canonical Allele Identifier: CA1204368234
Gene: LMX1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165318983C= , CM000663.2:g.165318983C= GRCh38
NC_000001.10:g.165288220C= , CM000663.1:g.165288220C= GRCh37
NC_000001.9:g.163554844C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000294816.6:c.263+34093G= ENSP00000294816.2:n.263+34093G=
ENST00000342310.7:c.263+34093G= MANE Select ENSP00000340226.3:n.263+34093G=
ENST00000367893.4:c.263+34093G= ENSP00000356868.4:n.263+34093G=
NM_001174069.1:c.263+34093G= NP_001167540.1:n.263+34093G=
NM_177398.3:c.263+34093G= NP_796372.1:n.263+34093G=
XM_011509540.1:c.263+34093G= XP_011507842.1:n.263+34093G=
XM_011509540.2:c.263+34093G= XP_011507842.1:n.263+34093G=
NM_177398.4:c.263+34093G= MANE Select NP_796372.1:n.263+34093G=
NM_001174069.2:c.263+34093G= NP_001167540.1:n.263+34093G=