Canonical Allele Identifier: CA2341394988

Gene: SIGLEC8

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51457590T= , CM000681.2:g.51457590T=	GRCh38
NC_000019.9:g.51960844T= , CM000681.1:g.51960844T=	GRCh37
NC_000019.8:g.56652656T=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000321424.7:c.604A= MANE Select	ENSP00000321077.2:p.Thr202=
ENST00000340550.5:c.454+344A=	ENSP00000339448.4:n.454+344A=
ENST00000430817.5:c.454+344A=	ENSP00000389142.1:n.454+344A=
ENST00000597352.1:n.220A=
NM_014442.2:c.604A=	NP_055257.2:p.Thr202=
XM_011526734.1:c.571A=	XP_011525036.1:p.Thr191=
XM_011526735.1:c.454+344A=	XP_011525037.1:n.454+344A=
NM_001363548.1:c.454+344A=	NP_001350477.1:n.454+344A=
XM_011526734.2:c.571A=	XP_011525036.1:p.Thr191=
NM_014442.3:c.604A= MANE Select	NP_055257.2:p.Thr202=