Canonical Allele Identifier: CA2685280242

Gene: CLEC5A MGAM OR9A4

Linked Data

• gnomAD v4: 7-141927373-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141927373G>T , CM000669.2:g.141927373G>T	GRCh38
NC_000007.13:g.141627173G>T , CM000669.1:g.141627173G>T	GRCh37
NC_000007.12:g.141273642G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000546910.6:c.*2731C>A (CLEC5A) MANE Select	ENSP00000449999.1:n.*2731C>A
ENST00000465654.5:c.-179-18448G>T (MGAM)	ENSP00000419372.1:n.-179-18448G>T
ENST00000497554.1:n.37-2404G>T (MGAM)
ENST00000546910.5:c.*2731C>A (CLEC5A)	ENSP00000449999.1:n.*2731C>A
NM_001301167.1:c.*2731C>A (CLEC5A)	NP_001288096.1:n.*2731C>A
NM_013252.2:c.*2731C>A (CLEC5A)	NP_037384.1:n.*2731C>A
XM_011515783.1:c.*24+7529G>T (OR9A4)	XP_011514085.1:n.*24+7529G>T
XM_011515995.1:c.*2731C>A (CLEC5A)	XP_011514297.1:n.*2731C>A
XR_927428.1:n.2682C>A (CLEC5A)
XM_011515995.2:c.*2731C>A (CLEC5A)	XP_011514297.1:n.*2731C>A
XM_017011915.1:c.*2731C>A (CLEC5A)	XP_016867404.1:n.*2731C>A
XM_017011917.1:c.*2799C>A (CLEC5A)	XP_016867406.1:n.*2799C>A
NM_013252.3:c.*2731C>A (CLEC5A) MANE Select	NP_037384.1:n.*2731C>A
NM_001301167.2:c.*2731C>A (CLEC5A)	NP_001288096.1:n.*2731C>A