Canonical Allele Identifier: CA1920786930

Gene: LRMDA

Linked Data

• dbSNP Id: rs10740455

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.76151274A>G , CM000672.2:g.76151274A>G	GRCh38
NC_000010.10:g.77911032A>G , CM000672.1:g.77911032A>G	GRCh37
NC_000010.9:g.77581038A>G	NCBI36
NG_042180.1:g.724629A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000611255.5:c.516+92491A>G MANE Select	ENSP00000480240.1:n.516+92491A>G
ENST00000372499.5:c.432+92491A>G	ENSP00000361577.1:n.432+92491A>G
ENST00000593699.5:n.870+92491A>G
ENST00000611255.4:c.516+92491A>G	ENSP00000480240.1:n.516+92491A>G
NM_001305581.1:c.516+92491A>G	NP_001292510.1:n.516+92491A>G
NM_032024.3:c.432+92491A>G	NP_114413.1:n.432+92491A>G
NM_032024.4:c.432+92491A>G	NP_114413.1:n.432+92491A>G
NR_131178.1:n.870+92491A>G
XM_011540256.1:c.516+92491A>G	XP_011538558.1:n.516+92491A>G
XM_011540257.1:c.516+92491A>G	XP_011538559.1:n.516+92491A>G
XM_011540258.1:c.516+92491A>G	XP_011538560.1:n.516+92491A>G
XR_945833.1:n.783+92491A>G
NM_001305581.2:c.516+92491A>G MANE Select	NP_001292510.1:n.516+92491A>G
NM_032024.5:c.432+92491A>G	NP_114413.1:n.432+92491A>G
NR_131178.2:n.870+92491A>G