Canonical Allele Identifier: CA13160445

Gene: LRMDA

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.76555466G>A , CM000672.2:g.76555466G>A	GRCh38
NC_000010.10:g.78315224G>A , CM000672.1:g.78315224G>A	GRCh37
NC_000010.9:g.77985230G>A	NCBI36
NG_042180.1:g.1128821G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000611255.5:c.602-1743G>A MANE Select	ENSP00000480240.1:n.602-1743G>A
ENST00000372499.5:c.518-1743G>A	ENSP00000361577.1:n.518-1743G>A
ENST00000468134.1:n.91-1743G>A
ENST00000483375.1:n.147-1743G>A
ENST00000488655.5:n.210-1743G>A
ENST00000488759.5:n.194-1743G>A
ENST00000493194.2:n.115-1743G>A
ENST00000496424.2:c.89-1743G>A	ENSP00000472558.1:n.89-1743G>A
ENST00000593699.5:n.956-1743G>A
ENST00000595936.1:n.209-1743G>A
ENST00000596228.5:n.243-1743G>A
ENST00000597823.1:n.238-1743G>A
ENST00000598708.1:n.276-1743G>A
ENST00000611255.4:c.602-1743G>A	ENSP00000480240.1:n.602-1743G>A
NM_001305581.1:c.602-1743G>A	NP_001292510.1:n.602-1743G>A
NM_032024.3:c.518-1743G>A	NP_114413.1:n.518-1743G>A
NM_032024.4:c.518-1743G>A	NP_114413.1:n.518-1743G>A
NR_131178.1:n.956-1743G>A
XM_011540257.1:c.517-1743G>A	XP_011538559.1:n.517-1743G>A
XR_945833.1:n.993-1743G>A
NM_001305581.2:c.602-1743G>A MANE Select	NP_001292510.1:n.602-1743G>A
NM_032024.5:c.518-1743G>A	NP_114413.1:n.518-1743G>A
NR_131178.2:n.956-1743G>A