Canonical Allele Identifier: CA10618622

Gene: SNCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89726489A>C , CM000666.2:g.89726489A>C	GRCh38
NC_000004.11:g.90647640A>C , CM000666.1:g.90647640A>C	GRCh37
NC_000004.10:g.90866663A>C	NCBI36
NG_011851.1:g.116808T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000394991.8:c.*139T>G MANE Select	ENSP00000378442.4:n.*139T>G
ENST00000673718.1:c.*139T>G	ENSP00000500990.1:n.*139T>G
ENST00000673766.1:n.817T>G
ENST00000673902.1:c.390+2705T>G	ENSP00000501102.1:n.390+2705T>G
ENST00000674129.1:c.*139T>G	ENSP00000501269.1:n.*139T>G
ENST00000336904.7:c.*139T>G	ENSP00000338345.3:n.*139T>G
ENST00000345009.8:c.*139T>G	ENSP00000343683.4:n.*139T>G
ENST00000394986.5:c.*139T>G	ENSP00000378437.1:n.*139T>G
ENST00000394989.6:c.*139T>G	ENSP00000378440.2:n.*139T>G
ENST00000394991.7:c.*139T>G	ENSP00000378442.3:n.*139T>G
ENST00000420646.6:c.*139T>G	ENSP00000396241.2:n.*139T>G
ENST00000508895.5:c.*139T>G	ENSP00000426955.1:n.*139T>G
ENST00000618500.4:c.*139T>G	ENSP00000484044.1:n.*139T>G
NM_000345.3:c.*139T>G	NP_000336.1:n.*139T>G
NM_001146054.1:c.*139T>G	NP_001139526.1:n.*139T>G
NM_001146055.1:c.*139T>G	NP_001139527.1:n.*139T>G
NM_007308.2:c.*139T>G	NP_009292.1:n.*139T>G
XM_011532208.1:c.*139T>G	XP_011530510.1:n.*139T>G
XM_011532208.2:c.*139T>G	XP_011530510.1:n.*139T>G
XM_017008562.1:c.*139T>G	XP_016864051.1:n.*139T>G
XM_017008563.1:c.*139T>G	XP_016864052.1:n.*139T>G
NM_000345.4:c.*139T>G MANE Select	NP_000336.1:n.*139T>G
NM_001146054.2:c.*139T>G	NP_001139526.1:n.*139T>G
NM_001146055.2:c.*139T>G	NP_001139527.1:n.*139T>G
NM_001375285.1:c.*139T>G	NP_001362214.1:n.*139T>G
NM_001375286.1:c.*139T>G	NP_001362215.1:n.*139T>G
NM_001375287.1:c.*139T>G	NP_001362216.1:n.*139T>G
NM_001375288.1:c.*139T>G	NP_001362217.1:n.*139T>G
NM_001375290.1:c.*139T>G	NP_001362219.1:n.*139T>G
NR_164674.1:n.640T>G
NR_164675.1:n.787T>G
NR_164676.1:n.860T>G
NM_007308.3:c.*139T>G	NP_009292.1:n.*139T>G