Canonical Allele Identifier: CA101497470
Gene: SNCA HGNC NCBI

Linked Data

dbSNP Id: rs145304567
gnomAD v3: 4-89726551-G-A
gnomAD v4: 4-89726551-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.89726551G>A , CM000666.2:g.89726551G>A GRCh38
NC_000004.11:g.90647702G>A , CM000666.1:g.90647702G>A GRCh37
NC_000004.10:g.90866725G>A NCBI36
NG_011851.1:g.116746C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000394991.8:c.*77C>T MANE Select ENSP00000378442.4:n.*77C>T
ENST00000673718.1:c.*77C>T ENSP00000500990.1:n.*77C>T
ENST00000673766.1:n.755C>T
ENST00000673902.1:c.390+2643C>T ENSP00000501102.1:n.390+2643C>T
ENST00000674129.1:c.*77C>T ENSP00000501269.1:n.*77C>T
ENST00000336904.7:c.*77C>T ENSP00000338345.3:n.*77C>T
ENST00000345009.8:c.*77C>T ENSP00000343683.4:n.*77C>T
ENST00000394986.5:c.*77C>T ENSP00000378437.1:n.*77C>T
ENST00000394989.6:c.*77C>T ENSP00000378440.2:n.*77C>T
ENST00000394991.7:c.*77C>T ENSP00000378442.3:n.*77C>T
ENST00000420646.6:c.*77C>T ENSP00000396241.2:n.*77C>T
ENST00000508895.5:c.*77C>T ENSP00000426955.1:n.*77C>T
ENST00000618500.4:c.*77C>T ENSP00000484044.1:n.*77C>T
NM_000345.3:c.*77C>T NP_000336.1:n.*77C>T
NM_001146054.1:c.*77C>T NP_001139526.1:n.*77C>T
NM_001146055.1:c.*77C>T NP_001139527.1:n.*77C>T
NM_007308.2:c.*77C>T NP_009292.1:n.*77C>T
XM_011532208.1:c.*77C>T XP_011530510.1:n.*77C>T
XM_011532208.2:c.*77C>T XP_011530510.1:n.*77C>T
XM_017008562.1:c.*77C>T XP_016864051.1:n.*77C>T
XM_017008563.1:c.*77C>T XP_016864052.1:n.*77C>T
NM_000345.4:c.*77C>T MANE Select NP_000336.1:n.*77C>T
NM_001146054.2:c.*77C>T NP_001139526.1:n.*77C>T
NM_001146055.2:c.*77C>T NP_001139527.1:n.*77C>T
NM_001375285.1:c.*77C>T NP_001362214.1:n.*77C>T
NM_001375286.1:c.*77C>T NP_001362215.1:n.*77C>T
NM_001375287.1:c.*77C>T NP_001362216.1:n.*77C>T
NM_001375288.1:c.*77C>T NP_001362217.1:n.*77C>T
NM_001375290.1:c.*77C>T NP_001362219.1:n.*77C>T
NR_164674.1:n.578C>T
NR_164675.1:n.725C>T
NR_164676.1:n.798C>T
NM_007308.3:c.*77C>T NP_009292.1:n.*77C>T