Canonical Allele Identifier: CA360883574

Gene: SNCAIP

Linked Data

• COSMIC: COSM5011465 ; COSM5011466
• MyVariant Identifiers: chr5:g.121786641G>T (hg19) ; chr5:g.122450946G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122450946G>T , CM000667.2:g.122450946G>T	GRCh38
NC_000005.9:g.121786641G>T , CM000667.1:g.121786641G>T	GRCh37
NC_000005.8:g.121814540G>T	NCBI36
NG_011486.1:g.143822G>T
NG_011486.2:g.143822G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261368.13:c.2099G>T MANE Select	ENSP00000261368.8:p.Arg700Met
ENST00000261367.11:c.2240G>T	ENSP00000261367.7:p.Arg747Met
ENST00000261368.12:c.2099G>T	ENSP00000261368.8:p.Arg700Met
ENST00000379538.7:c.1001G>T	ENSP00000368854.3:p.Arg334Met
ENST00000395466.6:c.1227G>T	ENSP00000378849.2:n.1227G>T
ENST00000395469.6:c.2465G>T	ENSP00000378852.2:n.2465G>T
ENST00000414317.6:c.933G>T	ENSP00000394392.3:n.933G>T
ENST00000504884.6:c.1227G>T	ENSP00000426904.2:n.1227G>T
ENST00000508017.5:c.*846G>T	ENSP00000424338.1:n.*846G>T
ENST00000509023.5:c.*744G>T	ENSP00000427078.1:n.*744G>T
ENST00000509154.6:c.1919G>T	ENSP00000422106.2:p.Arg640Met
ENST00000510658.5:c.*901G>T	ENSP00000426526.1:n.*901G>T
ENST00000512146.6:c.1188G>T	ENSP00000423360.2:n.1188G>T
ENST00000512385.5:c.*846G>T	ENSP00000426280.1:n.*846G>T
ENST00000513719.1:n.1084G>T
ENST00000515215.6:c.1047G>T	ENSP00000427575.2:n.1047G>T
ENST00000542191.5:c.*846G>T	ENSP00000441681.2:n.*846G>T
NM_001242935.1:c.1001G>T	NP_001229864.1:p.Arg334Met
NM_001242935.2:c.1001G>T	NP_001229864.1:p.Arg334Met
NM_001308100.1:c.2240G>T	NP_001295029.1:p.Arg747Met
NM_001308105.1:c.1919G>T	NP_001295034.1:p.Arg640Met
NM_001308106.1:c.995G>T	NP_001295035.1:p.Arg332Met
NM_001308107.1:c.1001G>T	NP_001295036.1:p.Arg334Met
NM_001308108.1:c.1181G>T	NP_001295037.1:p.Arg394Met
NM_001308109.1:c.887G>T	NP_001295038.1:p.Arg296Met
NM_005460.2:c.2099G>T	NP_005451.2:p.Arg700Met
NM_005460.3:c.2099G>T	NP_005451.2:p.Arg700Met
NR_051996.1:n.464-280C>A
NR_131761.1:n.2511G>T
NR_131762.1:n.1240G>T
XM_005272138.3:c.2099G>T	XP_005272195.1:p.Arg700Met
XM_005272139.1:c.2099G>T	XP_005272196.1:p.Arg700Met
XM_006714734.2:c.2099G>T	XP_006714797.1:p.Arg700Met
XM_011543736.1:c.2240G>T	XP_011542038.1:p.Arg747Met
XM_011543737.1:c.2240G>T	XP_011542039.1:p.Arg747Met
XM_011543738.1:c.2240G>T	XP_011542040.1:p.Arg747Met
XM_011543739.1:c.2240G>T	XP_011542041.1:p.Arg747Met
XM_011543741.1:c.2240G>T	XP_011542043.1:p.Arg747Met
XM_011543742.1:c.2240G>T	XP_011542044.1:p.Arg747Met
XM_011543743.1:c.2240G>T	XP_011542045.1:p.Arg747Met
XM_011543744.1:c.2240G>T	XP_011542046.1:p.Arg747Met
XM_011543745.1:c.2099G>T	XP_011542047.1:p.Arg700Met
XM_011543746.1:c.2240G>T	XP_011542048.1:p.Arg747Met
XM_011543747.1:c.2060G>T	XP_011542049.1:p.Arg687Met
XM_011543748.1:c.1919G>T	XP_011542050.1:p.Arg640Met
XM_011543749.1:c.1019G>T	XP_011542051.1:p.Arg340Met
XM_011543750.1:c.995G>T	XP_011542052.1:p.Arg332Met
XM_005272138.4:c.2099G>T	XP_005272195.1:p.Arg700Met
XM_011543737.2:c.2240G>T	XP_011542039.1:p.Arg747Met
XM_011543738.2:c.2240G>T	XP_011542040.1:p.Arg747Met
XM_011543741.2:c.2240G>T	XP_011542043.1:p.Arg747Met
XM_011543743.2:c.2240G>T	XP_011542045.1:p.Arg747Met
XM_011543749.2:c.1019G>T	XP_011542051.1:p.Arg340Met
XM_017010078.1:c.2240G>T	XP_016865567.1:p.Arg747Met
XM_017010079.1:c.2240G>T	XP_016865568.1:p.Arg747Met
XM_017010080.1:c.2240G>T	XP_016865569.1:p.Arg747Met
XM_017010081.1:c.2240G>T	XP_016865570.1:p.Arg747Met
XM_017010082.1:c.2099G>T	XP_016865571.1:p.Arg700Met
XM_017010083.1:c.1019G>T	XP_016865572.1:p.Arg340Met
XM_017010085.1:c.995G>T	XP_016865574.1:p.Arg332Met
XM_024446266.1:c.2099G>T	XP_024302034.1:p.Arg700Met
XM_024446267.1:c.2099G>T	XP_024302035.1:p.Arg700Met
XM_024446268.1:c.2099G>T	XP_024302036.1:p.Arg700Met
XM_024446269.1:c.1019G>T	XP_024302037.1:p.Arg340Met
XR_001742362.1:n.2653G>T
NM_005460.4:c.2099G>T MANE Select	NP_005451.2:p.Arg700Met
NM_001308100.2:c.2240G>T	NP_001295029.1:p.Arg747Met
NM_001308107.2:c.1001G>T	NP_001295036.1:p.Arg334Met
NM_001308109.2:c.887G>T	NP_001295038.1:p.Arg296Met
NM_001242935.3:c.1001G>T	NP_001229864.1:p.Arg334Met