Canonical Allele Identifier: CA1475362602

Gene: SNCA

Linked Data

• dbSNP Id: rs1732057347

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89784271_89784273del , CM000666.2:g.89784271_89784273del	GRCh38
NC_000004.11:g.90705422_90705424del , CM000666.1:g.90705422_90705424del	GRCh37
NC_000004.10:g.90924445_90924447del	NCBI36
NG_011851.1:g.59026_59028del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394991.8:c.306+37975_306+37977del MANE Select	ENSP00000378442.4:n.306+37975_306+37977del
ENST00000673718.1:c.306+37975_306+37977del	ENSP00000500990.1:n.306+37975_306+37977del
ENST00000673902.1:c.306+37975_306+37977del	ENSP00000501102.1:n.306+37975_306+37977del
ENST00000674129.1:c.307-24978_307-24976del	ENSP00000501269.1:n.307-24978_307-24976del
ENST00000336904.7:c.306+37975_306+37977del	ENSP00000338345.3:n.306+37975_306+37977del
ENST00000345009.8:c.306+37975_306+37977del	ENSP00000343683.4:n.306+37975_306+37977del
ENST00000394986.5:c.306+37975_306+37977del	ENSP00000378437.1:n.306+37975_306+37977del
ENST00000394989.6:c.264+37975_264+37977del	ENSP00000378440.2:n.264+37975_264+37977del
ENST00000394991.7:c.306+37975_306+37977del	ENSP00000378442.3:n.306+37975_306+37977del
ENST00000420646.6:c.306+37975_306+37977del	ENSP00000396241.2:n.306+37975_306+37977del
ENST00000505199.5:c.264+37975_264+37977del	ENSP00000421485.1:n.264+37975_264+37977del
ENST00000506244.5:c.306+37975_306+37977del	ENSP00000422238.1:n.306+37975_306+37977del
ENST00000508895.5:c.306+37975_306+37977del	ENSP00000426955.1:n.306+37975_306+37977del
ENST00000611107.1:c.264+37975_264+37977del	ENSP00000479604.1:n.264+37975_264+37977del
ENST00000618500.4:c.264+37975_264+37977del	ENSP00000484044.1:n.264+37975_264+37977del
NM_000345.3:c.306+37975_306+37977del	NP_000336.1:n.306+37975_306+37977del
NM_001146054.1:c.306+37975_306+37977del	NP_001139526.1:n.306+37975_306+37977del
NM_001146055.1:c.306+37975_306+37977del	NP_001139527.1:n.306+37975_306+37977del
NM_007308.2:c.306+37975_306+37977del	NP_009292.1:n.306+37975_306+37977del
XM_011532208.1:c.306+37975_306+37977del	XP_011530510.1:n.306+37975_306+37977del
XM_011532208.2:c.306+37975_306+37977del	XP_011530510.1:n.306+37975_306+37977del
XM_017008562.1:c.306+37975_306+37977del	XP_016864051.1:n.306+37975_306+37977del
XM_017008563.1:c.306+37975_306+37977del	XP_016864052.1:n.306+37975_306+37977del
NM_000345.4:c.306+37975_306+37977del MANE Select	NP_000336.1:n.306+37975_306+37977del
NM_001146054.2:c.306+37975_306+37977del	NP_001139526.1:n.306+37975_306+37977del
NM_001146055.2:c.306+37975_306+37977del	NP_001139527.1:n.306+37975_306+37977del
NM_001375285.1:c.306+37975_306+37977del	NP_001362214.1:n.306+37975_306+37977del
NM_001375286.1:c.306+37975_306+37977del	NP_001362215.1:n.306+37975_306+37977del
NM_001375287.1:c.306+37975_306+37977del	NP_001362216.1:n.306+37975_306+37977del
NM_001375288.1:c.306+37975_306+37977del	NP_001362217.1:n.306+37975_306+37977del
NR_164674.1:n.384+37975_384+37977del
NR_164675.1:n.531+37975_531+37977del
NR_164676.1:n.604+37975_604+37977del
NM_007308.3:c.306+37975_306+37977del	NP_009292.1:n.306+37975_306+37977del