Canonical Allele Identifier: CA1748228079

Gene: CLEC5A MGAM OR9A4

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141927385A= , CM000669.2:g.141927385A=	GRCh38
NC_000007.13:g.141627185A= , CM000669.1:g.141627185A=	GRCh37
NC_000007.12:g.141273654A=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000546910.6:c.*2719T= (CLEC5A) MANE Select	ENSP00000449999.1:n.*2719T=
ENST00000465654.5:c.-179-18436A= (MGAM)	ENSP00000419372.1:n.-179-18436A=
ENST00000497554.1:n.37-2392A= (MGAM)
ENST00000546910.5:c.*2719T= (CLEC5A)	ENSP00000449999.1:n.*2719T=
NM_001301167.1:c.*2719T= (CLEC5A)	NP_001288096.1:n.*2719T=
NM_013252.2:c.*2719T= (CLEC5A)	NP_037384.1:n.*2719T=
XM_011515783.1:c.*24+7541A= (OR9A4)	XP_011514085.1:n.*24+7541A=
XM_011515995.1:c.*2719T= (CLEC5A)	XP_011514297.1:n.*2719T=
XR_927428.1:n.2670T= (CLEC5A)
XM_011515995.2:c.*2719T= (CLEC5A)	XP_011514297.1:n.*2719T=
XM_017011915.1:c.*2719T= (CLEC5A)	XP_016867404.1:n.*2719T=
XM_017011917.1:c.*2787T= (CLEC5A)	XP_016867406.1:n.*2787T=
NM_013252.3:c.*2719T= (CLEC5A) MANE Select	NP_037384.1:n.*2719T=
NM_001301167.2:c.*2719T= (CLEC5A)	NP_001288096.1:n.*2719T=