Canonical Allele Identifier: CA2341395041

Gene: SIGLEC8

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51457686A= , CM000681.2:g.51457686A=	GRCh38
NC_000019.9:g.51960940A= , CM000681.1:g.51960940A=	GRCh37
NC_000019.8:g.56652752A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_014442.3:c.508T= MANE Select	NP_055257.2:p.Ser170=
ENST00000321424.7:c.508T= MANE Select	ENSP00000321077.2:p.Ser170=
NM_001363548.1:c.454+248T=	NP_001350477.1:n.454+248T=
NM_014442.2:c.508T=	NP_055257.2:p.Ser170=
ENST00000340550.5:c.454+248T=	ENSP00000339448.4:n.454+248T=
ENST00000430817.5:c.454+248T=	ENSP00000389142.1:n.454+248T=
ENST00000597352.1:n.124T=
XM_011526734.1:c.475T=	XP_011525036.1:p.Ser159=
XM_011526734.2:c.475T=	XP_011525036.1:p.Ser159=
XM_011526735.1:c.454+248T=	XP_011525037.1:n.454+248T=