Canonical Allele Identifier: CA3069694439

Gene: SYP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49191328A= , CM000685.2:g.49191328A=	GRCh38
NC_000023.10:g.49047785A= , CM000685.1:g.49047785A=	GRCh37
NC_000023.9:g.48934729A=	NCBI36
NG_012532.1:g.13877T=

Transcript Alleles

HGVS	Amino-acid Change
NM_003179.3:c.*4+105T= MANE Select	NP_003170.1:n.*4+105T=
ENST00000263233.9:c.*4+105T= MANE Select	ENSP00000263233.4:n.*4+105T=
NM_003179.2:c.*4+105T=	NP_003170.1:n.*4+105T=
ENST00000263233.8:c.*4+105T=	ENSP00000263233.4:n.*4+105T=
ENST00000376303.6:c.*698+105T=	ENSP00000365480.2:n.*698+105T=
ENST00000472598.5:c.615+105T=
ENST00000479808.5:c.*109T=	ENSP00000418169.1:n.*109T=
ENST00000689634.1:n.2638T=
ENST00000692723.1:n.972+105T=
XM_011543950.1:c.*4+105T=	XP_011542252.1:n.*4+105T=
XM_011543951.1:c.*4+105T=	XP_011542253.1:n.*4+105T=