Canonical Allele Identifier: CA101497498

Gene: SNCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89726869_89726871dup , CM000666.2:g.89726869_89726871dup	GRCh38
NC_000004.11:g.90648020_90648022dup , CM000666.1:g.90648020_90648022dup	GRCh37
NC_000004.10:g.90867043_90867045dup	NCBI36
NG_011851.1:g.116432_116434dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394991.8:c.391-205_391-203dup MANE Select	ENSP00000378442.4:n.391-205_391-203dup
ENST00000673718.1:c.391-205_391-203dup	ENSP00000500990.1:n.391-205_391-203dup
ENST00000673766.1:n.646-205_646-203dup
ENST00000673902.1:c.390+2329_390+2331dup	ENSP00000501102.1:n.390+2329_390+2331dup
ENST00000674129.1:c.448-205_448-203dup	ENSP00000501269.1:n.448-205_448-203dup
ENST00000336904.7:c.391-205_391-203dup	ENSP00000338345.3:n.391-205_391-203dup
ENST00000345009.8:c.307-205_307-203dup	ENSP00000343683.4:n.307-205_307-203dup
ENST00000394986.5:c.391-205_391-203dup	ENSP00000378437.1:n.391-205_391-203dup
ENST00000394989.6:c.349-205_349-203dup	ENSP00000378440.2:n.349-205_349-203dup
ENST00000394991.7:c.391-205_391-203dup	ENSP00000378442.3:n.391-205_391-203dup
ENST00000420646.6:c.307-205_307-203dup	ENSP00000396241.2:n.307-205_307-203dup
ENST00000505199.5:c.349-205_349-203dup	ENSP00000421485.1:n.349-205_349-203dup
ENST00000506244.5:c.391-205_391-203dup	ENSP00000422238.1:n.391-205_391-203dup
ENST00000508895.5:c.391-205_391-203dup	ENSP00000426955.1:n.391-205_391-203dup
ENST00000611107.1:c.265-205_265-203dup	ENSP00000479604.1:n.265-205_265-203dup
ENST00000618500.4:c.349-205_349-203dup	ENSP00000484044.1:n.349-205_349-203dup
NM_000345.3:c.391-205_391-203dup	NP_000336.1:n.391-205_391-203dup
NM_001146054.1:c.391-205_391-203dup	NP_001139526.1:n.391-205_391-203dup
NM_001146055.1:c.391-205_391-203dup	NP_001139527.1:n.391-205_391-203dup
NM_007308.2:c.307-205_307-203dup	NP_009292.1:n.307-205_307-203dup
XM_011532208.1:c.391-205_391-203dup	XP_011530510.1:n.391-205_391-203dup
XM_011532208.2:c.391-205_391-203dup	XP_011530510.1:n.391-205_391-203dup
XM_017008562.1:c.391-205_391-203dup	XP_016864051.1:n.391-205_391-203dup
XM_017008563.1:c.391-205_391-203dup	XP_016864052.1:n.391-205_391-203dup
NM_000345.4:c.391-205_391-203dup MANE Select	NP_000336.1:n.391-205_391-203dup
NM_001146054.2:c.391-205_391-203dup	NP_001139526.1:n.391-205_391-203dup
NM_001146055.2:c.391-205_391-203dup	NP_001139527.1:n.391-205_391-203dup
NM_001375285.1:c.391-205_391-203dup	NP_001362214.1:n.391-205_391-203dup
NM_001375286.1:c.391-205_391-203dup	NP_001362215.1:n.391-205_391-203dup
NM_001375287.1:c.391-205_391-203dup	NP_001362216.1:n.391-205_391-203dup
NM_001375288.1:c.391-205_391-203dup	NP_001362217.1:n.391-205_391-203dup
NM_001375290.1:c.247-205_247-203dup	NP_001362219.1:n.247-205_247-203dup
NR_164674.1:n.469-205_469-203dup
NR_164675.1:n.616-205_616-203dup
NR_164676.1:n.689-205_689-203dup
NM_007308.3:c.307-205_307-203dup	NP_009292.1:n.307-205_307-203dup