Canonical Allele Identifier: CA3069694455

Gene: SYP

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49191415C= , CM000685.2:g.49191415C=	GRCh38
NC_000023.10:g.49047872C= , CM000685.1:g.49047872C=	GRCh37
NC_000023.9:g.48934816C=	NCBI36
NG_012532.1:g.13790G=

Transcript Alleles

HGVS	Amino-acid Change
NM_003179.3:c.*4+18G= MANE Select	NP_003170.1:n.*4+18G=
ENST00000263233.9:c.*4+18G= MANE Select	ENSP00000263233.4:n.*4+18G=
NM_003179.2:c.*4+18G=	NP_003170.1:n.*4+18G=
ENST00000263233.8:c.*4+18G=	ENSP00000263233.4:n.*4+18G=
ENST00000376303.6:c.*698+18G=	ENSP00000365480.2:n.*698+18G=
ENST00000472598.5:c.615+18G=
ENST00000479808.5:c.*22G=	ENSP00000418169.1:n.*22G=
ENST00000689634.1:n.2551G=
ENST00000692723.1:n.972+18G=
XM_011543950.1:c.*4+18G=	XP_011542252.1:n.*4+18G=
XM_011543951.1:c.*4+18G=	XP_011542253.1:n.*4+18G=