Canonical Allele Identifier: CA1204368382
Gene: LMX1A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.165319147T= , CM000663.2:g.165319147T= GRCh38
NC_000001.10:g.165288384T= , CM000663.1:g.165288384T= GRCh37
NC_000001.9:g.163555008T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000294816.6:c.263+33929A= ENSP00000294816.2:n.263+33929A=
ENST00000342310.7:c.263+33929A= MANE Select ENSP00000340226.3:n.263+33929A=
ENST00000367893.4:c.263+33929A= ENSP00000356868.4:n.263+33929A=
NM_001174069.1:c.263+33929A= NP_001167540.1:n.263+33929A=
NM_177398.3:c.263+33929A= NP_796372.1:n.263+33929A=
XM_011509540.1:c.263+33929A= XP_011507842.1:n.263+33929A=
XM_011509540.2:c.263+33929A= XP_011507842.1:n.263+33929A=
NM_177398.4:c.263+33929A= MANE Select NP_796372.1:n.263+33929A=
NM_001174069.2:c.263+33929A= NP_001167540.1:n.263+33929A=
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