Canonical Allele Identifier: CA360882981

Gene: SNCAIP

Linked Data

• MyVariant Identifiers: chr5:g.121786434A>C (hg19) ; chr5:g.122450739A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122450739A>C , CM000667.2:g.122450739A>C	GRCh38
NC_000005.9:g.121786434A>C , CM000667.1:g.121786434A>C	GRCh37
NC_000005.8:g.121814333A>C	NCBI36
NG_011486.1:g.143615A>C
NG_011486.2:g.143615A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261368.13:c.1892A>C MANE Select	ENSP00000261368.8:p.Asn631Thr
ENST00000261367.11:c.2033A>C	ENSP00000261367.7:p.Asn678Thr
ENST00000261368.12:c.1892A>C	ENSP00000261368.8:p.Asn631Thr
ENST00000379538.7:c.794A>C	ENSP00000368854.3:p.Asn265Thr
ENST00000395466.6:c.1020A>C	ENSP00000378849.2:n.1020A>C
ENST00000395469.6:c.2258A>C	ENSP00000378852.2:n.2258A>C
ENST00000414317.6:c.726A>C	ENSP00000394392.3:n.726A>C
ENST00000504884.6:c.1020A>C	ENSP00000426904.2:n.1020A>C
ENST00000508017.5:c.*639A>C	ENSP00000424338.1:n.*639A>C
ENST00000509023.5:c.*537A>C	ENSP00000427078.1:n.*537A>C
ENST00000509154.6:c.1712A>C	ENSP00000422106.2:p.Asn571Thr
ENST00000510658.5:c.*694A>C	ENSP00000426526.1:n.*694A>C
ENST00000512146.6:c.981A>C	ENSP00000423360.2:n.981A>C
ENST00000512385.5:c.*639A>C	ENSP00000426280.1:n.*639A>C
ENST00000513719.1:n.877A>C
ENST00000515215.6:c.840A>C	ENSP00000427575.2:n.840A>C
ENST00000542191.5:c.*639A>C	ENSP00000441681.2:n.*639A>C
NM_001242935.1:c.794A>C	NP_001229864.1:p.Asn265Thr
NM_001242935.2:c.794A>C	NP_001229864.1:p.Asn265Thr
NM_001308100.1:c.2033A>C	NP_001295029.1:p.Asn678Thr
NM_001308105.1:c.1712A>C	NP_001295034.1:p.Asn571Thr
NM_001308106.1:c.788A>C	NP_001295035.1:p.Asn263Thr
NM_001308107.1:c.794A>C	NP_001295036.1:p.Asn265Thr
NM_001308108.1:c.974A>C	NP_001295037.1:p.Asn325Thr
NM_001308109.1:c.680A>C	NP_001295038.1:p.Asn227Thr
NM_005460.2:c.1892A>C	NP_005451.2:p.Asn631Thr
NM_005460.3:c.1892A>C	NP_005451.2:p.Asn631Thr
NR_051996.1:n.464-73T>G
NR_131761.1:n.2304A>C
NR_131762.1:n.1033A>C
XM_005272138.3:c.1892A>C	XP_005272195.1:p.Asn631Thr
XM_005272139.1:c.1892A>C	XP_005272196.1:p.Asn631Thr
XM_006714734.2:c.1892A>C	XP_006714797.1:p.Asn631Thr
XM_011543736.1:c.2033A>C	XP_011542038.1:p.Asn678Thr
XM_011543737.1:c.2033A>C	XP_011542039.1:p.Asn678Thr
XM_011543738.1:c.2033A>C	XP_011542040.1:p.Asn678Thr
XM_011543739.1:c.2033A>C	XP_011542041.1:p.Asn678Thr
XM_011543741.1:c.2033A>C	XP_011542043.1:p.Asn678Thr
XM_011543742.1:c.2033A>C	XP_011542044.1:p.Asn678Thr
XM_011543743.1:c.2033A>C	XP_011542045.1:p.Asn678Thr
XM_011543744.1:c.2033A>C	XP_011542046.1:p.Asn678Thr
XM_011543745.1:c.1892A>C	XP_011542047.1:p.Asn631Thr
XM_011543746.1:c.2033A>C	XP_011542048.1:p.Asn678Thr
XM_011543747.1:c.1853A>C	XP_011542049.1:p.Asn618Thr
XM_011543748.1:c.1712A>C	XP_011542050.1:p.Asn571Thr
XM_011543749.1:c.812A>C	XP_011542051.1:p.Asn271Thr
XM_011543750.1:c.788A>C	XP_011542052.1:p.Asn263Thr
XM_005272138.4:c.1892A>C	XP_005272195.1:p.Asn631Thr
XM_011543737.2:c.2033A>C	XP_011542039.1:p.Asn678Thr
XM_011543738.2:c.2033A>C	XP_011542040.1:p.Asn678Thr
XM_011543741.2:c.2033A>C	XP_011542043.1:p.Asn678Thr
XM_011543743.2:c.2033A>C	XP_011542045.1:p.Asn678Thr
XM_011543749.2:c.812A>C	XP_011542051.1:p.Asn271Thr
XM_017010078.1:c.2033A>C	XP_016865567.1:p.Asn678Thr
XM_017010079.1:c.2033A>C	XP_016865568.1:p.Asn678Thr
XM_017010080.1:c.2033A>C	XP_016865569.1:p.Asn678Thr
XM_017010081.1:c.2033A>C	XP_016865570.1:p.Asn678Thr
XM_017010082.1:c.1892A>C	XP_016865571.1:p.Asn631Thr
XM_017010083.1:c.812A>C	XP_016865572.1:p.Asn271Thr
XM_017010085.1:c.788A>C	XP_016865574.1:p.Asn263Thr
XM_024446266.1:c.1892A>C	XP_024302034.1:p.Asn631Thr
XM_024446267.1:c.1892A>C	XP_024302035.1:p.Asn631Thr
XM_024446268.1:c.1892A>C	XP_024302036.1:p.Asn631Thr
XM_024446269.1:c.812A>C	XP_024302037.1:p.Asn271Thr
XR_001742362.1:n.2446A>C
NM_005460.4:c.1892A>C MANE Select	NP_005451.2:p.Asn631Thr
NM_001308100.2:c.2033A>C	NP_001295029.1:p.Asn678Thr
NM_001308107.2:c.794A>C	NP_001295036.1:p.Asn265Thr
NM_001308109.2:c.680A>C	NP_001295038.1:p.Asn227Thr
NM_001242935.3:c.794A>C	NP_001229864.1:p.Asn265Thr