Canonical Allele Identifier: CA916330347

Gene: LMX1A

Linked Data

• dbSNP Id: rs1553212138

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165319039_165319043del , CM000663.2:g.165319039_165319043del	GRCh38
NC_000001.10:g.165288276_165288280del , CM000663.1:g.165288276_165288280del	GRCh37
NC_000001.9:g.163554900_163554904del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294816.6:c.263+34034_263+34038del	ENSP00000294816.2:n.263+34034_263+34038del
ENST00000342310.7:c.263+34034_263+34038del MANE Select	ENSP00000340226.3:n.263+34034_263+34038del
ENST00000367893.4:c.263+34034_263+34038del	ENSP00000356868.4:n.263+34034_263+34038del
NM_001174069.1:c.263+34034_263+34038del	NP_001167540.1:n.263+34034_263+34038del
NM_177398.3:c.263+34034_263+34038del	NP_796372.1:n.263+34034_263+34038del
XM_011509540.1:c.263+34034_263+34038del	XP_011507842.1:n.263+34034_263+34038del
XM_011509540.2:c.263+34034_263+34038del	XP_011507842.1:n.263+34034_263+34038del
NM_177398.4:c.263+34034_263+34038del MANE Select	NP_796372.1:n.263+34034_263+34038del
NM_001174069.2:c.263+34034_263+34038del	NP_001167540.1:n.263+34034_263+34038del