Canonical Allele Identifier: CA1065252095
Gene: SNCA HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89725550_89725551insTTTTTTTTTTG , CM000666.2:g.89725550_89725551insTTTTTTTTTTG GRCh38
NC_000004.11:g.90646701_90646702insTTTTTTTTTTG , CM000666.1:g.90646701_90646702insTTTTTTTTTTG GRCh37
NC_000004.10:g.90865724_90865725insTTTTTTTTTTG NCBI36
NG_011851.1:g.117746_117747insCAAAAAAAAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000394991.8:c.*1077_*1078insCAAAAAAAAAA MANE Select ENSP00000378442.4:n.*1077_*1078insCAAAAAAAAAA
ENST00000673718.1:c.*1077_*1078insCAAAAAAAAAA ENSP00000500990.1:n.*1077_*1078insCAAAAAAAAAA
ENST00000673766.1:n.1755_1756insCAAAAAAAAAA
ENST00000673902.1:c.390+3643_390+3644insCAAAAAAAAAA ENSP00000501102.1:n.390+3643_390+3644insCAAAAAAAAAA
ENST00000674129.1:c.*1077_*1078insCAAAAAAAAAA ENSP00000501269.1:n.*1077_*1078insCAAAAAAAAAA
ENST00000336904.7:c.*1077_*1078insCAAAAAAAAAA ENSP00000338345.3:n.*1077_*1078insCAAAAAAAAAA
ENST00000394989.6:c.*1077_*1078insCAAAAAAAAAA ENSP00000378440.2:n.*1077_*1078insCAAAAAAAAAA
ENST00000420646.6:c.*1077_*1078insCAAAAAAAAAA ENSP00000396241.2:n.*1077_*1078insCAAAAAAAAAA
ENST00000618500.4:c.*1077_*1078insCAAAAAAAAAA ENSP00000484044.1:n.*1077_*1078insCAAAAAAAAAA
NM_000345.3:c.*1077_*1078insCAAAAAAAAAA NP_000336.1:n.*1077_*1078insCAAAAAAAAAA
NM_001146054.1:c.*1077_*1078insCAAAAAAAAAA NP_001139526.1:n.*1077_*1078insCAAAAAAAAAA
NM_001146055.1:c.*1077_*1078insCAAAAAAAAAA NP_001139527.1:n.*1077_*1078insCAAAAAAAAAA
NM_007308.2:c.*1077_*1078insCAAAAAAAAAA NP_009292.1:n.*1077_*1078insCAAAAAAAAAA
XM_011532208.1:c.*1077_*1078insCAAAAAAAAAA XP_011530510.1:n.*1077_*1078insCAAAAAAAAAA
XM_011532208.2:c.*1077_*1078insCAAAAAAAAAA XP_011530510.1:n.*1077_*1078insCAAAAAAAAAA
XM_017008562.1:c.*1077_*1078insCAAAAAAAAAA XP_016864051.1:n.*1077_*1078insCAAAAAAAAAA
XM_017008563.1:c.*1077_*1078insCAAAAAAAAAA XP_016864052.1:n.*1077_*1078insCAAAAAAAAAA
NM_000345.4:c.*1077_*1078insCAAAAAAAAAA MANE Select NP_000336.1:n.*1077_*1078insCAAAAAAAAAA
NM_001146054.2:c.*1077_*1078insCAAAAAAAAAA NP_001139526.1:n.*1077_*1078insCAAAAAAAAAA
NM_001146055.2:c.*1077_*1078insCAAAAAAAAAA NP_001139527.1:n.*1077_*1078insCAAAAAAAAAA
NM_001375285.1:c.*1077_*1078insCAAAAAAAAAA NP_001362214.1:n.*1077_*1078insCAAAAAAAAAA
NM_001375286.1:c.*1077_*1078insCAAAAAAAAAA NP_001362215.1:n.*1077_*1078insCAAAAAAAAAA
NM_001375287.1:c.*1077_*1078insCAAAAAAAAAA NP_001362216.1:n.*1077_*1078insCAAAAAAAAAA
NM_001375288.1:c.*1077_*1078insCAAAAAAAAAA NP_001362217.1:n.*1077_*1078insCAAAAAAAAAA
NM_001375290.1:c.*1077_*1078insCAAAAAAAAAA NP_001362219.1:n.*1077_*1078insCAAAAAAAAAA
NR_164674.1:n.1277-237_1277-236insCAAAAAAAAAA
NR_164675.1:n.1424-237_1424-236insCAAAAAAAAAA
NR_164676.1:n.1798_1799insCAAAAAAAAAA
NM_007308.3:c.*1077_*1078insCAAAAAAAAAA NP_009292.1:n.*1077_*1078insCAAAAAAAAAA