Canonical Allele Identifier: CA10619899

Gene: SNCAIP

Linked Data

• ClinVar Variation Id: 350479
• ClinVar RCV Id: RCV000311066
• dbSNP Id: rs192969505
• gnomAD v2: 5-121647977-C-G
• gnomAD v3: 5-122312282-C-G
• gnomAD v4: 5-122312282-C-G
• MyVariant Identifiers: chr5:g.121647977C>G (hg19) ; chr5:g.122312282C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122312282C>G , CM000667.2:g.122312282C>G	GRCh38
NC_000005.9:g.121647977C>G , CM000667.1:g.121647977C>G	GRCh37
NC_000005.8:g.121675876C>G	NCBI36
NG_011486.1:g.5158C>G
NG_011486.2:g.5158C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261368.13:c.-49C>G MANE Select	ENSP00000261368.8:n.-49C>G
ENST00000261367.11:c.-1353C>G	ENSP00000261367.7:n.-1353C>G
ENST00000261368.12:c.-49C>G	ENSP00000261368.8:n.-49C>G
ENST00000379538.7:c.-95C>G	ENSP00000368854.3:n.-95C>G
ENST00000506272.5:c.-47+485C>G	ENSP00000426551.1:n.-47+485C>G
ENST00000508017.5:c.-49C>G	ENSP00000424338.1:n.-49C>G
ENST00000508681.5:c.-47+444C>G	ENSP00000422610.1:n.-47+444C>G
ENST00000509023.5:c.-49C>G	ENSP00000427078.1:n.-49C>G
ENST00000509154.6:c.-164+444C>G	ENSP00000422106.2:n.-164+444C>G
ENST00000510003.5:n.46C>G
ENST00000510658.5:c.-47+500C>G	ENSP00000426526.1:n.-47+500C>G
ENST00000512385.5:c.-49C>G	ENSP00000426280.1:n.-49C>G
ENST00000514467.5:c.-47+657C>G	ENSP00000427090.1:n.-47+657C>G
ENST00000514497.6:c.-166C>G	ENSP00000425063.2:n.-166C>G
ENST00000542191.5:c.-49C>G	ENSP00000441681.2:n.-49C>G
NM_001242935.1:c.-95C>G	NP_001229864.1:n.-95C>G
NM_001242935.2:c.-95C>G	NP_001229864.1:n.-95C>G
NM_001308100.1:c.-1353C>G	NP_001295029.1:n.-1353C>G
NM_001308107.1:c.-95C>G	NP_001295036.1:n.-95C>G
NM_001308109.1:c.-95C>G	NP_001295038.1:n.-95C>G
NM_005460.2:c.-49C>G	NP_005451.2:n.-49C>G
NM_005460.3:c.-49C>G	NP_005451.2:n.-49C>G
NR_131762.1:n.92+500C>G
XM_005272138.3:c.-49C>G	XP_005272195.1:n.-49C>G
XM_005272139.1:c.-47+444C>G	XP_005272196.1:n.-47+444C>G
XM_006714734.2:c.-47+657C>G	XP_006714797.1:n.-47+657C>G
XM_011543736.1:c.-47+444C>G	XP_011542038.1:n.-47+444C>G
XM_011543737.1:c.-49C>G	XP_011542039.1:n.-49C>G
XM_011543738.1:c.-47+500C>G	XP_011542040.1:n.-47+500C>G
XM_011543739.1:c.-47+485C>G	XP_011542041.1:n.-47+485C>G
XM_011543742.1:c.-47+657C>G	XP_011542044.1:n.-47+657C>G
XM_011543744.1:c.-47+444C>G	XP_011542046.1:n.-47+444C>G
XM_011543746.1:c.-47+444C>G	XP_011542048.1:n.-47+444C>G
XM_011543747.1:c.-47+444C>G	XP_011542049.1:n.-47+444C>G
XM_011543748.1:c.-49C>G	XP_011542050.1:n.-49C>G
XM_005272138.4:c.-49C>G	XP_005272195.1:n.-49C>G
XM_011543737.2:c.-49C>G	XP_011542039.1:n.-49C>G
XM_011543738.2:c.-47+500C>G	XP_011542040.1:n.-47+500C>G
XM_017010079.1:c.-49C>G	XP_016865568.1:n.-49C>G
XM_017010080.1:c.-49C>G	XP_016865569.1:n.-49C>G
XM_017010081.1:c.-49C>G	XP_016865570.1:n.-49C>G
XM_017010083.1:c.-75+500C>G	XP_016865572.1:n.-75+500C>G
XM_017010084.1:c.-49C>G	XP_016865573.1:n.-49C>G
XM_017010085.1:c.-240+444C>G	XP_016865574.1:n.-240+444C>G
XM_017010086.1:c.-49C>G	XP_016865575.1:n.-49C>G
XM_024446266.1:c.-47+500C>G	XP_024302034.1:n.-47+500C>G
XM_024446267.1:c.-47+500C>G	XP_024302035.1:n.-47+500C>G
XM_024446268.1:c.-47+485C>G	XP_024302036.1:n.-47+485C>G
XM_024446269.1:c.-75+500C>G	XP_024302037.1:n.-75+500C>G
XR_001742362.1:n.140C>G
XR_001742363.1:n.136C>G
XR_001742364.1:n.136C>G
XR_001742365.2:n.136C>G
XR_001742366.1:n.135C>G
NM_005460.4:c.-49C>G MANE Select	NP_005451.2:n.-49C>G
NM_001308100.2:c.-1353C>G	NP_001295029.1:n.-1353C>G
NM_001308107.2:c.-95C>G	NP_001295036.1:n.-95C>G
NM_001308109.2:c.-95C>G	NP_001295038.1:n.-95C>G
NM_001242935.3:c.-95C>G	NP_001229864.1:n.-95C>G