Canonical Allele Identifier: CA3066643600

Gene: SYP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49191335G= , CM000685.2:g.49191335G=	GRCh38
NC_000023.10:g.49047792G= , CM000685.1:g.49047792G=	GRCh37
NC_000023.9:g.48934736G=	NCBI36
NG_012532.1:g.13870C=

Transcript Alleles

HGVS	Amino-acid Change
NM_003179.3:c.*4+98C= MANE Select	NP_003170.1:n.*4+98C=
ENST00000263233.9:c.*4+98C= MANE Select	ENSP00000263233.4:n.*4+98C=
NM_003179.2:c.*4+98C=	NP_003170.1:n.*4+98C=
ENST00000263233.8:c.*4+98C=	ENSP00000263233.4:n.*4+98C=
ENST00000376303.6:c.*698+98C=	ENSP00000365480.2:n.*698+98C=
ENST00000472598.5:c.615+98C=
ENST00000479808.5:c.*102C=	ENSP00000418169.1:n.*102C=
ENST00000689634.1:n.2631C=
ENST00000692723.1:n.972+98C=
XM_011543950.1:c.*4+98C=	XP_011542252.1:n.*4+98C=
XM_011543951.1:c.*4+98C=	XP_011542253.1:n.*4+98C=