Canonical Allele Identifier: CA2341292931

Gene: CD33

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.51235662G= , CM000681.2:g.51235662G=	GRCh38
NC_000019.9:g.51738917G= , CM000681.1:g.51738917G=	GRCh37
NC_000019.8:g.56430729G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001772.4:c.910G= MANE Select	NP_001763.3:p.Gly304=
ENST00000262262.5:c.910G= MANE Select	ENSP00000262262.3:p.Gly304=
NM_001082618.1:c.529G=	NP_001076087.1:p.Gly177=
NM_001082618.2:c.529G=	NP_001076087.1:p.Gly177=
NM_001177608.1:c.910G=	NP_001171079.1:p.Gly304=
NM_001177608.2:c.910G=	NP_001171079.1:p.Gly304=
NM_001772.3:c.910G=	NP_001763.3:p.Gly304=
ENST00000262262.4:c.910G=	ENSP00000262262.3:p.Gly304=
ENST00000391796.7:c.910G=	ENSP00000375673.2:p.Gly304=
ENST00000421133.6:c.529G=	ENSP00000410126.1:p.Gly177=
ENST00000436584.6:c.529G=	ENSP00000403331.2:p.Gly177=
ENST00000598473.1:n.281G=
ENST00000601785.5:n.1037G=
XM_011527531.1:c.1072G=	XP_011525833.1:p.Gly358=
XM_011527531.2:c.1072G=	XP_011525833.1:p.Gly358=
XM_011527532.1:c.910G=	XP_011525834.1:p.Gly304=
XM_011527532.2:c.910G=	XP_011525834.1:p.Gly304=
XM_017027508.1:c.1072G=	XP_016882997.1:p.Gly358=
XM_017027509.1:c.1024G=	XP_016882998.1:p.Gly342=
XM_017027510.1:c.691G=	XP_016882999.1:p.Gly231=
XR_935875.1:n.1144G=