Canonical Allele Identifier: CA360882706
Gene: SNCAIP HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.122450612C>A , CM000667.2:g.122450612C>A GRCh38
NC_000005.9:g.121786307C>A , CM000667.1:g.121786307C>A GRCh37
NC_000005.8:g.121814206C>A NCBI36
NG_011486.1:g.143488C>A
NG_011486.2:g.143488C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261368.13:c.1765C>A MANE Select ENSP00000261368.8:p.Pro589Thr
ENST00000261367.11:c.1906C>A ENSP00000261367.7:p.Pro636Thr
ENST00000261368.12:c.1765C>A ENSP00000261368.8:p.Pro589Thr
ENST00000379538.7:c.667C>A ENSP00000368854.3:p.Pro223Thr
ENST00000395466.6:c.893C>A ENSP00000378849.2:n.893C>A
ENST00000395469.6:c.2131C>A ENSP00000378852.2:n.2131C>A
ENST00000414317.6:c.599C>A ENSP00000394392.3:n.599C>A
ENST00000504884.6:c.893C>A ENSP00000426904.2:n.893C>A
ENST00000508017.5:c.*512C>A ENSP00000424338.1:n.*512C>A
ENST00000509023.5:c.*410C>A ENSP00000427078.1:n.*410C>A
ENST00000509154.6:c.1585C>A ENSP00000422106.2:p.Pro529Thr
ENST00000510658.5:c.*567C>A ENSP00000426526.1:n.*567C>A
ENST00000512146.6:c.854C>A ENSP00000423360.2:n.854C>A
ENST00000512385.5:c.*512C>A ENSP00000426280.1:n.*512C>A
ENST00000513719.1:n.750C>A
ENST00000515215.6:c.713C>A ENSP00000427575.2:n.713C>A
ENST00000542191.5:c.*512C>A ENSP00000441681.2:n.*512C>A
NM_001242935.1:c.667C>A NP_001229864.1:p.Pro223Thr
NM_001242935.2:c.667C>A NP_001229864.1:p.Pro223Thr
NM_001308100.1:c.1906C>A NP_001295029.1:p.Pro636Thr
NM_001308105.1:c.1585C>A NP_001295034.1:p.Pro529Thr
NM_001308106.1:c.661C>A NP_001295035.1:p.Pro221Thr
NM_001308107.1:c.667C>A NP_001295036.1:p.Pro223Thr
NM_001308108.1:c.847C>A NP_001295037.1:p.Pro283Thr
NM_001308109.1:c.553C>A NP_001295038.1:p.Pro185Thr
NM_005460.2:c.1765C>A NP_005451.2:p.Pro589Thr
NM_005460.3:c.1765C>A NP_005451.2:p.Pro589Thr
NR_051996.1:n.518G>T
NR_131761.1:n.2177C>A
NR_131762.1:n.906C>A
XM_005272138.3:c.1765C>A XP_005272195.1:p.Pro589Thr
XM_005272139.1:c.1765C>A XP_005272196.1:p.Pro589Thr
XM_006714734.2:c.1765C>A XP_006714797.1:p.Pro589Thr
XM_011543736.1:c.1906C>A XP_011542038.1:p.Pro636Thr
XM_011543737.1:c.1906C>A XP_011542039.1:p.Pro636Thr
XM_011543738.1:c.1906C>A XP_011542040.1:p.Pro636Thr
XM_011543739.1:c.1906C>A XP_011542041.1:p.Pro636Thr
XM_011543741.1:c.1906C>A XP_011542043.1:p.Pro636Thr
XM_011543742.1:c.1906C>A XP_011542044.1:p.Pro636Thr
XM_011543743.1:c.1906C>A XP_011542045.1:p.Pro636Thr
XM_011543744.1:c.1906C>A XP_011542046.1:p.Pro636Thr
XM_011543745.1:c.1765C>A XP_011542047.1:p.Pro589Thr
XM_011543746.1:c.1906C>A XP_011542048.1:p.Pro636Thr
XM_011543747.1:c.1726C>A XP_011542049.1:p.Pro576Thr
XM_011543748.1:c.1585C>A XP_011542050.1:p.Pro529Thr
XM_011543749.1:c.685C>A XP_011542051.1:p.Pro229Thr
XM_011543750.1:c.661C>A XP_011542052.1:p.Pro221Thr
XM_005272138.4:c.1765C>A XP_005272195.1:p.Pro589Thr
XM_011543737.2:c.1906C>A XP_011542039.1:p.Pro636Thr
XM_011543738.2:c.1906C>A XP_011542040.1:p.Pro636Thr
XM_011543741.2:c.1906C>A XP_011542043.1:p.Pro636Thr
XM_011543743.2:c.1906C>A XP_011542045.1:p.Pro636Thr
XM_011543749.2:c.685C>A XP_011542051.1:p.Pro229Thr
XM_017010078.1:c.1906C>A XP_016865567.1:p.Pro636Thr
XM_017010079.1:c.1906C>A XP_016865568.1:p.Pro636Thr
XM_017010080.1:c.1906C>A XP_016865569.1:p.Pro636Thr
XM_017010081.1:c.1906C>A XP_016865570.1:p.Pro636Thr
XM_017010082.1:c.1765C>A XP_016865571.1:p.Pro589Thr
XM_017010083.1:c.685C>A XP_016865572.1:p.Pro229Thr
XM_017010085.1:c.661C>A XP_016865574.1:p.Pro221Thr
XM_024446266.1:c.1765C>A XP_024302034.1:p.Pro589Thr
XM_024446267.1:c.1765C>A XP_024302035.1:p.Pro589Thr
XM_024446268.1:c.1765C>A XP_024302036.1:p.Pro589Thr
XM_024446269.1:c.685C>A XP_024302037.1:p.Pro229Thr
XR_001742362.1:n.2319C>A
NM_005460.4:c.1765C>A MANE Select NP_005451.2:p.Pro589Thr
NM_001308100.2:c.1906C>A NP_001295029.1:p.Pro636Thr
NM_001308107.2:c.667C>A NP_001295036.1:p.Pro223Thr
NM_001308109.2:c.553C>A NP_001295038.1:p.Pro185Thr
NM_001242935.3:c.667C>A NP_001229864.1:p.Pro223Thr