Canonical Allele Identifier: CA168098022

Gene: CLEC5A MGAM OR9A4

Linked Data

• dbSNP Id: rs535428832
• gnomAD v3: 7-141927359-G-A
• gnomAD v4: 7-141927359-G-A
• MyVariant Identifiers: chr7:g.141627159G>A (hg19) ; chr7:g.141927359G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141927359G>A , CM000669.2:g.141927359G>A	GRCh38
NC_000007.13:g.141627159G>A , CM000669.1:g.141627159G>A	GRCh37
NC_000007.12:g.141273628G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000546910.6:c.*2745C>T (CLEC5A) MANE Select	ENSP00000449999.1:n.*2745C>T
ENST00000465654.5:c.-179-18462G>A (MGAM)	ENSP00000419372.1:n.-179-18462G>A
ENST00000497554.1:n.37-2418G>A (MGAM)
ENST00000546910.5:c.*2745C>T (CLEC5A)	ENSP00000449999.1:n.*2745C>T
NM_001301167.1:c.*2745C>T (CLEC5A)	NP_001288096.1:n.*2745C>T
NM_013252.2:c.*2745C>T (CLEC5A)	NP_037384.1:n.*2745C>T
XM_011515783.1:c.*24+7515G>A (OR9A4)	XP_011514085.1:n.*24+7515G>A
XM_011515995.1:c.*2745C>T (CLEC5A)	XP_011514297.1:n.*2745C>T
XR_927428.1:n.2696C>T (CLEC5A)
XM_011515995.2:c.*2745C>T (CLEC5A)	XP_011514297.1:n.*2745C>T
XM_017011915.1:c.*2745C>T (CLEC5A)	XP_016867404.1:n.*2745C>T
XM_017011917.1:c.*2813C>T (CLEC5A)	XP_016867406.1:n.*2813C>T
NM_013252.3:c.*2745C>T (CLEC5A) MANE Select	NP_037384.1:n.*2745C>T
NM_001301167.2:c.*2745C>T (CLEC5A)	NP_001288096.1:n.*2745C>T