Canonical Allele Identifier: CA1475337374

Gene: SNCA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.89725770A= , CM000666.2:g.89725770A=	GRCh38
NC_000004.11:g.90646921A= , CM000666.1:g.90646921A=	GRCh37
NC_000004.10:g.90865944A=	NCBI36
NG_011851.1:g.117527T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000394991.8:c.*858T= MANE Select	ENSP00000378442.4:n.*858T=
ENST00000673718.1:c.*858T=	ENSP00000500990.1:n.*858T=
ENST00000673766.1:n.1536T=
ENST00000673902.1:c.390+3424T=	ENSP00000501102.1:n.390+3424T=
ENST00000674129.1:c.*858T=	ENSP00000501269.1:n.*858T=
ENST00000336904.7:c.*858T=	ENSP00000338345.3:n.*858T=
ENST00000394989.6:c.*858T=	ENSP00000378440.2:n.*858T=
ENST00000420646.6:c.*858T=	ENSP00000396241.2:n.*858T=
ENST00000618500.4:c.*858T=	ENSP00000484044.1:n.*858T=
NM_000345.3:c.*858T=	NP_000336.1:n.*858T=
NM_001146054.1:c.*858T=	NP_001139526.1:n.*858T=
NM_001146055.1:c.*858T=	NP_001139527.1:n.*858T=
NM_007308.2:c.*858T=	NP_009292.1:n.*858T=
XM_011532208.1:c.*858T=	XP_011530510.1:n.*858T=
XM_011532208.2:c.*858T=	XP_011530510.1:n.*858T=
XM_017008562.1:c.*858T=	XP_016864051.1:n.*858T=
XM_017008563.1:c.*858T=	XP_016864052.1:n.*858T=
NM_000345.4:c.*858T= MANE Select	NP_000336.1:n.*858T=
NM_001146054.2:c.*858T=	NP_001139526.1:n.*858T=
NM_001146055.2:c.*858T=	NP_001139527.1:n.*858T=
NM_001375285.1:c.*858T=	NP_001362214.1:n.*858T=
NM_001375286.1:c.*858T=	NP_001362215.1:n.*858T=
NM_001375287.1:c.*858T=	NP_001362216.1:n.*858T=
NM_001375288.1:c.*858T=	NP_001362217.1:n.*858T=
NM_001375290.1:c.*858T=	NP_001362219.1:n.*858T=
NR_164674.1:n.1276+83T=
NR_164675.1:n.1423+83T=
NR_164676.1:n.1579T=
NM_007308.3:c.*858T=	NP_009292.1:n.*858T=