Canonical Allele Identifier: CA1204368334

Gene: LMX1A

Linked Data

• dbSNP Id: rs1655305534

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.165319040_165319041insCC , CM000663.2:g.165319040_165319041insCC	GRCh38
NC_000001.10:g.165288277_165288278insCC , CM000663.1:g.165288277_165288278insCC	GRCh37
NC_000001.9:g.163554901_163554902insCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294816.6:c.263+34036_263+34037insGG	ENSP00000294816.2:n.263+34036_263+34037insGG
ENST00000342310.7:c.263+34036_263+34037insGG MANE Select	ENSP00000340226.3:n.263+34036_263+34037insGG
ENST00000367893.4:c.263+34036_263+34037insGG	ENSP00000356868.4:n.263+34036_263+34037insGG
NM_001174069.1:c.263+34036_263+34037insGG	NP_001167540.1:n.263+34036_263+34037insGG
NM_177398.3:c.263+34036_263+34037insGG	NP_796372.1:n.263+34036_263+34037insGG
XM_011509540.1:c.263+34036_263+34037insGG	XP_011507842.1:n.263+34036_263+34037insGG
XM_011509540.2:c.263+34036_263+34037insGG	XP_011507842.1:n.263+34036_263+34037insGG
NM_177398.4:c.263+34036_263+34037insGG MANE Select	NP_796372.1:n.263+34036_263+34037insGG
NM_001174069.2:c.263+34036_263+34037insGG	NP_001167540.1:n.263+34036_263+34037insGG