Canonical Allele Identifier: CA578284276

Gene: CLEC5A MGAM OR9A4

Linked Data

• dbSNP Id: rs1554439674
• gnomAD v2: 7-141627176-T-C
• gnomAD v3: 7-141927376-T-C
• gnomAD v4: 7-141927376-T-C
• MyVariant Identifiers: chr7:g.141627176T>C (hg19) ; chr7:g.141927376T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.141927376T>C , CM000669.2:g.141927376T>C	GRCh38
NC_000007.13:g.141627176T>C , CM000669.1:g.141627176T>C	GRCh37
NC_000007.12:g.141273645T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000546910.6:c.*2728A>G (CLEC5A) MANE Select	ENSP00000449999.1:n.*2728A>G
ENST00000465654.5:c.-179-18445T>C (MGAM)	ENSP00000419372.1:n.-179-18445T>C
ENST00000497554.1:n.37-2401T>C (MGAM)
ENST00000546910.5:c.*2728A>G (CLEC5A)	ENSP00000449999.1:n.*2728A>G
NM_001301167.1:c.*2728A>G (CLEC5A)	NP_001288096.1:n.*2728A>G
NM_013252.2:c.*2728A>G (CLEC5A)	NP_037384.1:n.*2728A>G
XM_011515783.1:c.*24+7532T>C (OR9A4)	XP_011514085.1:n.*24+7532T>C
XM_011515995.1:c.*2728A>G (CLEC5A)	XP_011514297.1:n.*2728A>G
XR_927428.1:n.2679A>G (CLEC5A)
XM_011515995.2:c.*2728A>G (CLEC5A)	XP_011514297.1:n.*2728A>G
XM_017011915.1:c.*2728A>G (CLEC5A)	XP_016867404.1:n.*2728A>G
XM_017011917.1:c.*2796A>G (CLEC5A)	XP_016867406.1:n.*2796A>G
NM_013252.3:c.*2728A>G (CLEC5A) MANE Select	NP_037384.1:n.*2728A>G
NM_001301167.2:c.*2728A>G (CLEC5A)	NP_001288096.1:n.*2728A>G