Canonical Allele Identifier: CA2547332987
Gene: SNCA HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89725234_89725235insAATGAGTGACTATAAGGATGGTTA , CM000666.2:g.89725234_89725235insAATGAGTGACTATAAGGATGGTTA GRCh38
NC_000004.11:g.90646385_90646386insAATGAGTGACTATAAGGATGGTTA , CM000666.1:g.90646385_90646386insAATGAGTGACTATAAGGATGGTTA GRCh37
NC_000004.10:g.90865408_90865409insAATGAGTGACTATAAGGATGGTTA NCBI36
NG_011851.1:g.118062_118063insTAACCATCCTTATAGTCACTCATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000394991.8:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT MANE Select ENSP00000378442.4:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
ENST00000673718.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT ENSP00000500990.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
ENST00000673766.1:n.2071_2072insTAACCATCCTTATAGTCACTCATT
ENST00000673902.1:c.390+3959_390+3960insTAACCATCCTTATAGTCACTCATT ENSP00000501102.1:n.390+3959_390+3960insTAACCATCCTTATAGTCACTC...
ENST00000336904.7:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT ENSP00000338345.3:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
ENST00000394989.6:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT ENSP00000378440.2:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
ENST00000420646.6:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT ENSP00000396241.2:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
ENST00000618500.4:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT ENSP00000484044.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_000345.3:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_000336.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001146054.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001139526.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001146055.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001139527.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_007308.2:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_009292.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_000345.4:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT MANE Select NP_000336.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001146054.2:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001139526.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001146055.2:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001139527.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001375285.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001362214.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001375286.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001362215.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001375287.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001362216.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001375288.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001362217.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NM_001375290.1:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_001362219.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT
NR_164674.1:n.1356_1357insTAACCATCCTTATAGTCACTCATT
NR_164675.1:n.1503_1504insTAACCATCCTTATAGTCACTCATT
NR_164676.1:n.2114_2115insTAACCATCCTTATAGTCACTCATT
NM_007308.3:c.*1393_*1394insTAACCATCCTTATAGTCACTCATT NP_009292.1:n.*1393_*1394insTAACCATCCTTATAGTCACTCATT