Canonical Allele Identifier: CA10621979

Gene: SNCA

Linked Data

• ClinVar Variation Id: 350089
• ClinVar RCV Id: RCV000312446
• dbSNP Id: rs886059724
• gnomAD v2: 4-90646701-TA-T
• gnomAD v3: 4-89725550-TA-T
• gnomAD v4: 4-89725550-TA-T
• MyVariant Identifiers: chr4:g.90646702del (hg19) ; chr4:g.89725551del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89725551del , CM000666.2:g.89725551del	GRCh38
NC_000004.11:g.90646702del , CM000666.1:g.90646702del	GRCh37
NC_000004.10:g.90865725del	NCBI36
NG_011851.1:g.117746del

Transcript Alleles

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