Canonical Allele Identifier: CA1140173839

Gene: SYPL2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.109479215T= , CM000663.2:g.109479215T=	GRCh38
NC_000001.10:g.110021837T= , CM000663.1:g.110021837T=	GRCh37
NC_000001.9:g.109823360T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001040709.2:c.649-163T= MANE Select	NP_001035799.1:n.649-163T=
ENST00000369872.4:c.649-163T= MANE Select	ENSP00000358888.3:n.649-163T=
NM_001040709.1:c.649-163T=	NP_001035799.1:n.649-163T=
ENST00000369872.3:c.649-163T=	ENSP00000358888.3:n.649-163T=
XM_005270773.3:c.*4-163T=	XP_005270830.1:n.*4-163T=
XM_011541283.1:c.649-163T=	XP_011539585.1:n.649-163T=
XM_011541283.2:c.649-163T=	XP_011539585.1:n.649-163T=
XM_011541284.1:c.457-163T=	XP_011539586.1:n.457-163T=
XM_011541284.2:c.457-163T=	XP_011539586.1:n.457-163T=
XM_011541285.1:c.457-163T=	XP_011539587.1:n.457-163T=