Canonical Allele Identifier: CA309804464

Gene: SIGLEC5

Linked Data

• dbSNP Id: rs962781726
• MyVariant Identifiers: chr19:g.52127693G>A (hg19) ; chr19:g.51624440G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51624440G>A , CM000681.2:g.51624440G>A	GRCh38
NC_000019.9:g.52127693G>A , CM000681.1:g.52127693G>A	GRCh37
NC_000019.8:g.56819505G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000683636.1:c.1464+1592C>T MANE Select	ENSP00000507738.1:n.1464+1592C>T
ENST00000429354.3:c.1464+1592C>T	ENSP00000415200.2:n.1464+1592C>T
ENST00000534261.3:c.1464+1592C>T	ENSP00000473238.1:n.1464+1592C>T
ENST00000570106.6:c.1464+1592C>T	ENSP00000455510.2:n.1464+1592C>T
ENST00000599649.5:c.1464+1592C>T	ENSP00000470259.1:n.1464+1592C>T
NM_003830.3:c.1464+1592C>T	NP_003821.1:n.1464+1592C>T
XM_011527438.1:c.1382+2709C>T	XP_011525740.1:n.1382+2709C>T
XM_011527438.2:c.1382+2709C>T	XP_011525740.1:n.1382+2709C>T
XM_017027419.1:c.1491+1592C>T	XP_016882908.1:n.1491+1592C>T
NM_001384708.1:c.1382+2709C>T	NP_001371637.1:n.1382+2709C>T
NM_001384709.1:c.1179+1592C>T	NP_001371638.1:n.1179+1592C>T
NM_003830.4:c.1464+1592C>T MANE Select	NP_003821.1:n.1464+1592C>T