Canonical Allele Identifier: CA2762579144

Gene: SNCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89725569T>G , CM000666.2:g.89725569T>G	GRCh38
NC_000004.11:g.90646720T>G , CM000666.1:g.90646720T>G	GRCh37
NC_000004.10:g.90865743T>G	NCBI36
NG_011851.1:g.117728A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000394991.8:c.*1059A>C MANE Select	ENSP00000378442.4:n.*1059A>C
ENST00000673718.1:c.*1059A>C	ENSP00000500990.1:n.*1059A>C
ENST00000673766.1:n.1737A>C
ENST00000673902.1:c.390+3625A>C	ENSP00000501102.1:n.390+3625A>C
ENST00000674129.1:c.*1059A>C	ENSP00000501269.1:n.*1059A>C
ENST00000336904.7:c.*1059A>C	ENSP00000338345.3:n.*1059A>C
ENST00000394989.6:c.*1059A>C	ENSP00000378440.2:n.*1059A>C
ENST00000420646.6:c.*1059A>C	ENSP00000396241.2:n.*1059A>C
ENST00000618500.4:c.*1059A>C	ENSP00000484044.1:n.*1059A>C
NM_000345.3:c.*1059A>C	NP_000336.1:n.*1059A>C
NM_001146054.1:c.*1059A>C	NP_001139526.1:n.*1059A>C
NM_001146055.1:c.*1059A>C	NP_001139527.1:n.*1059A>C
NM_007308.2:c.*1059A>C	NP_009292.1:n.*1059A>C
XM_011532208.1:c.*1059A>C	XP_011530510.1:n.*1059A>C
XM_011532208.2:c.*1059A>C	XP_011530510.1:n.*1059A>C
XM_017008562.1:c.*1059A>C	XP_016864051.1:n.*1059A>C
XM_017008563.1:c.*1059A>C	XP_016864052.1:n.*1059A>C
NM_000345.4:c.*1059A>C MANE Select	NP_000336.1:n.*1059A>C
NM_001146054.2:c.*1059A>C	NP_001139526.1:n.*1059A>C
NM_001146055.2:c.*1059A>C	NP_001139527.1:n.*1059A>C
NM_001375285.1:c.*1059A>C	NP_001362214.1:n.*1059A>C
NM_001375286.1:c.*1059A>C	NP_001362215.1:n.*1059A>C
NM_001375287.1:c.*1059A>C	NP_001362216.1:n.*1059A>C
NM_001375288.1:c.*1059A>C	NP_001362217.1:n.*1059A>C
NM_001375290.1:c.*1059A>C	NP_001362219.1:n.*1059A>C
NR_164674.1:n.1277-255A>C
NR_164675.1:n.1424-255A>C
NR_164676.1:n.1780A>C
NM_007308.3:c.*1059A>C	NP_009292.1:n.*1059A>C