Canonical Allele Identifier: CA2341473614
Gene: SIGLEC5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.51624166_51624206delinsATATATATTATAAGCAGGAAAAATGAATACAACTGCAACTT , CM000681.2:g.51624166_51624206delinsATATATATTATAAGCAGGAAAAATGAATACAACTGCAACTT GRCh38
NC_000019.9:g.52127419_52127459delinsATATATATTATAAGCAGGAAAAATGAATACAACTGCAACTT , CM000681.1:g.52127419_52127459delinsATATATATTATAAGCAGGAAAAATGAATACAACTGCAACTT GRCh37
NC_000019.8:g.56819231_56819271delinsATATATATTATAAGCAGGAAAAATGAATACAACTGCAACTT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000683636.1:c.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT MANE Select ENSP00000507738.1:n.1464+1826_1464+1866delinsAAGTTGCAGTTGTATT...
ENST00000429354.3:c.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT ENSP00000415200.2:n.1464+1826_1464+1866delinsAAGTTGCAGTTGTATT...
ENST00000534261.3:c.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT ENSP00000473238.1:n.1464+1826_1464+1866delinsAAGTTGCAGTTGTATT...
ENST00000570106.6:c.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT ENSP00000455510.2:n.1464+1826_1464+1866delinsAAGTTGCAGTTGTATT...
ENST00000599649.5:c.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT ENSP00000470259.1:n.1464+1826_1464+1866delinsAAGTTGCAGTTGTATT...
NM_003830.3:c.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT NP_003821.1:n.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTT...
XM_011527438.1:c.1382+2943_1382+2983delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT XP_011525740.1:n.1382+2943_1382+2983delinsAAGTTGCAGTTGTATTCAT...
XM_011527438.2:c.1382+2943_1382+2983delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT XP_011525740.1:n.1382+2943_1382+2983delinsAAGTTGCAGTTGTATTCAT...
XM_017027419.1:c.1491+1826_1491+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT XP_016882908.1:n.1491+1826_1491+1866delinsAAGTTGCAGTTGTATTCAT...
NM_001384708.1:c.1382+2943_1382+2983delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT NP_001371637.1:n.1382+2943_1382+2983delinsAAGTTGCAGTTGTATTCAT...
NM_001384709.1:c.1179+1826_1179+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT NP_001371638.1:n.1179+1826_1179+1866delinsAAGTTGCAGTTGTATTCAT...
NM_003830.4:c.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTTTCCTGCTTATAATATATAT MANE Select NP_003821.1:n.1464+1826_1464+1866delinsAAGTTGCAGTTGTATTCATTTT...