Canonical Allele Identifier: CA2814762987
Gene: SIGLEC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51624408_51624409insGC , CM000681.2:g.51624408_51624409insGC GRCh38
NC_000019.9:g.52127661_52127662insGC , CM000681.1:g.52127661_52127662insGC GRCh37
NC_000019.8:g.56819473_56819474insGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000683636.1:c.1464+1623_1464+1624insGC MANE Select ENSP00000507738.1:n.1464+1623_1464+1624insGC
ENST00000429354.3:c.1464+1623_1464+1624insGC ENSP00000415200.2:n.1464+1623_1464+1624insGC
ENST00000534261.3:c.1464+1623_1464+1624insGC ENSP00000473238.1:n.1464+1623_1464+1624insGC
ENST00000570106.6:c.1464+1623_1464+1624insGC ENSP00000455510.2:n.1464+1623_1464+1624insGC
ENST00000599649.5:c.1464+1623_1464+1624insGC ENSP00000470259.1:n.1464+1623_1464+1624insGC
NM_003830.3:c.1464+1623_1464+1624insGC NP_003821.1:n.1464+1623_1464+1624insGC
XM_011527438.1:c.1382+2740_1382+2741insGC XP_011525740.1:n.1382+2740_1382+2741insGC
XM_011527438.2:c.1382+2740_1382+2741insGC XP_011525740.1:n.1382+2740_1382+2741insGC
XM_017027419.1:c.1491+1623_1491+1624insGC XP_016882908.1:n.1491+1623_1491+1624insGC
NM_001384708.1:c.1382+2740_1382+2741insGC NP_001371637.1:n.1382+2740_1382+2741insGC
NM_001384709.1:c.1179+1623_1179+1624insGC NP_001371638.1:n.1179+1623_1179+1624insGC
NM_003830.4:c.1464+1623_1464+1624insGC MANE Select NP_003821.1:n.1464+1623_1464+1624insGC