Canonical Allele Identifier: CA633742767

Gene: SIGLEC5

Linked Data

• dbSNP Id: rs1253951609
• gnomAD v2: 19-52127500-A-G
• gnomAD v3: 19-51624247-A-G
• gnomAD v4: 19-51624247-A-G
• MyVariant Identifiers: chr19:g.52127500A>G (hg19) ; chr19:g.51624247A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51624247A>G , CM000681.2:g.51624247A>G	GRCh38
NC_000019.9:g.52127500A>G , CM000681.1:g.52127500A>G	GRCh37
NC_000019.8:g.56819312A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000683636.1:c.1464+1785T>C MANE Select	ENSP00000507738.1:n.1464+1785T>C
ENST00000429354.3:c.1464+1785T>C	ENSP00000415200.2:n.1464+1785T>C
ENST00000534261.3:c.1464+1785T>C	ENSP00000473238.1:n.1464+1785T>C
ENST00000570106.6:c.1464+1785T>C	ENSP00000455510.2:n.1464+1785T>C
ENST00000599649.5:c.1464+1785T>C	ENSP00000470259.1:n.1464+1785T>C
NM_003830.3:c.1464+1785T>C	NP_003821.1:n.1464+1785T>C
XM_011527438.1:c.1382+2902T>C	XP_011525740.1:n.1382+2902T>C
XM_011527438.2:c.1382+2902T>C	XP_011525740.1:n.1382+2902T>C
XM_017027419.1:c.1491+1785T>C	XP_016882908.1:n.1491+1785T>C
NM_001384708.1:c.1382+2902T>C	NP_001371637.1:n.1382+2902T>C
NM_001384709.1:c.1179+1785T>C	NP_001371638.1:n.1179+1785T>C
NM_003830.4:c.1464+1785T>C MANE Select	NP_003821.1:n.1464+1785T>C