Canonical Allele Identifier: CA996886594

Gene: SIGLEC5

Linked Data

• dbSNP Id: rs1983393985
• gnomAD v3: 19-51624166-ATATATATTATAAGCAGGAAAAATGAATACAACTGCAACTT-A
• gnomAD v4: 19-51624166-ATATATATTATAAGCAGGAAAAATGAATACAACTGCAACTT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51624171_51624210del , CM000681.2:g.51624171_51624210del	GRCh38
NC_000019.9:g.52127424_52127463del , CM000681.1:g.52127424_52127463del	GRCh37
NC_000019.8:g.56819236_56819275del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683636.1:c.1464+1826_1464+1865del MANE Select	ENSP00000507738.1:n.1464+1826_1464+1865del
ENST00000429354.3:c.1464+1826_1464+1865del	ENSP00000415200.2:n.1464+1826_1464+1865del
ENST00000534261.3:c.1464+1826_1464+1865del	ENSP00000473238.1:n.1464+1826_1464+1865del
ENST00000570106.6:c.1464+1826_1464+1865del	ENSP00000455510.2:n.1464+1826_1464+1865del
ENST00000599649.5:c.1464+1826_1464+1865del	ENSP00000470259.1:n.1464+1826_1464+1865del
NM_003830.3:c.1464+1826_1464+1865del	NP_003821.1:n.1464+1826_1464+1865del
XM_011527438.1:c.1382+2943_1382+2982del	XP_011525740.1:n.1382+2943_1382+2982del
XM_011527438.2:c.1382+2943_1382+2982del	XP_011525740.1:n.1382+2943_1382+2982del
XM_017027419.1:c.1491+1826_1491+1865del	XP_016882908.1:n.1491+1826_1491+1865del
NM_001384708.1:c.1382+2943_1382+2982del	NP_001371637.1:n.1382+2943_1382+2982del
NM_001384709.1:c.1179+1826_1179+1865del	NP_001371638.1:n.1179+1826_1179+1865del
NM_003830.4:c.1464+1826_1464+1865del MANE Select	NP_003821.1:n.1464+1826_1464+1865del