Canonical Allele Identifier: CA360883751

Gene: SNCAIP

Linked Data

• gnomAD v4: 5-122450999-C-T
• MyVariant Identifiers: chr5:g.121786694C>T (hg19) ; chr5:g.122450999C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.122450999C>T , CM000667.2:g.122450999C>T	GRCh38
NC_000005.9:g.121786694C>T , CM000667.1:g.121786694C>T	GRCh37
NC_000005.8:g.121814593C>T	NCBI36
NG_011486.1:g.143875C>T
NG_011486.2:g.143875C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261368.13:c.2152C>T MANE Select	ENSP00000261368.8:p.His718Tyr
ENST00000261367.11:c.2293C>T	ENSP00000261367.7:p.His765Tyr
ENST00000261368.12:c.2152C>T	ENSP00000261368.8:p.His718Tyr
ENST00000379538.7:c.1054C>T	ENSP00000368854.3:p.His352Tyr
ENST00000395466.6:c.1280C>T	ENSP00000378849.2:n.1280C>T
ENST00000395469.6:c.2518C>T	ENSP00000378852.2:n.2518C>T
ENST00000414317.6:c.986C>T	ENSP00000394392.3:n.986C>T
ENST00000504884.6:c.1280C>T	ENSP00000426904.2:n.1280C>T
ENST00000508017.5:c.*899C>T	ENSP00000424338.1:n.*899C>T
ENST00000509023.5:c.*797C>T	ENSP00000427078.1:n.*797C>T
ENST00000509154.6:c.1972C>T	ENSP00000422106.2:p.His658Tyr
ENST00000510658.5:c.*954C>T	ENSP00000426526.1:n.*954C>T
ENST00000512146.6:c.1241C>T	ENSP00000423360.2:n.1241C>T
ENST00000512385.5:c.*899C>T	ENSP00000426280.1:n.*899C>T
ENST00000513719.1:n.1137C>T
ENST00000515215.6:c.1100C>T	ENSP00000427575.2:n.1100C>T
ENST00000542191.5:c.*899C>T	ENSP00000441681.2:n.*899C>T
NM_001242935.1:c.1054C>T	NP_001229864.1:p.His352Tyr
NM_001242935.2:c.1054C>T	NP_001229864.1:p.His352Tyr
NM_001308100.1:c.2293C>T	NP_001295029.1:p.His765Tyr
NM_001308105.1:c.1972C>T	NP_001295034.1:p.His658Tyr
NM_001308106.1:c.1048C>T	NP_001295035.1:p.His350Tyr
NM_001308107.1:c.1054C>T	NP_001295036.1:p.His352Tyr
NM_001308108.1:c.1234C>T	NP_001295037.1:p.His412Tyr
NM_001308109.1:c.940C>T	NP_001295038.1:p.His314Tyr
NM_005460.2:c.2152C>T	NP_005451.2:p.His718Tyr
NM_005460.3:c.2152C>T	NP_005451.2:p.His718Tyr
NR_051996.1:n.464-333G>A
NR_131761.1:n.2564C>T
NR_131762.1:n.1293C>T
XM_005272138.3:c.2152C>T	XP_005272195.1:p.His718Tyr
XM_005272139.1:c.2152C>T	XP_005272196.1:p.His718Tyr
XM_006714734.2:c.2152C>T	XP_006714797.1:p.His718Tyr
XM_011543736.1:c.2293C>T	XP_011542038.1:p.His765Tyr
XM_011543737.1:c.2293C>T	XP_011542039.1:p.His765Tyr
XM_011543738.1:c.2293C>T	XP_011542040.1:p.His765Tyr
XM_011543739.1:c.2293C>T	XP_011542041.1:p.His765Tyr
XM_011543741.1:c.2293C>T	XP_011542043.1:p.His765Tyr
XM_011543742.1:c.2293C>T	XP_011542044.1:p.His765Tyr
XM_011543743.1:c.2293C>T	XP_011542045.1:p.His765Tyr
XM_011543744.1:c.2293C>T	XP_011542046.1:p.His765Tyr
XM_011543745.1:c.2152C>T	XP_011542047.1:p.His718Tyr
XM_011543746.1:c.2293C>T	XP_011542048.1:p.His765Tyr
XM_011543747.1:c.2113C>T	XP_011542049.1:p.His705Tyr
XM_011543748.1:c.1972C>T	XP_011542050.1:p.His658Tyr
XM_011543749.1:c.1072C>T	XP_011542051.1:p.His358Tyr
XM_011543750.1:c.1048C>T	XP_011542052.1:p.His350Tyr
XM_005272138.4:c.2152C>T	XP_005272195.1:p.His718Tyr
XM_011543737.2:c.2293C>T	XP_011542039.1:p.His765Tyr
XM_011543738.2:c.2293C>T	XP_011542040.1:p.His765Tyr
XM_011543741.2:c.2293C>T	XP_011542043.1:p.His765Tyr
XM_011543743.2:c.2293C>T	XP_011542045.1:p.His765Tyr
XM_011543749.2:c.1072C>T	XP_011542051.1:p.His358Tyr
XM_017010078.1:c.2293C>T	XP_016865567.1:p.His765Tyr
XM_017010079.1:c.2293C>T	XP_016865568.1:p.His765Tyr
XM_017010080.1:c.2293C>T	XP_016865569.1:p.His765Tyr
XM_017010081.1:c.2293C>T	XP_016865570.1:p.His765Tyr
XM_017010082.1:c.2152C>T	XP_016865571.1:p.His718Tyr
XM_017010083.1:c.1072C>T	XP_016865572.1:p.His358Tyr
XM_017010085.1:c.1048C>T	XP_016865574.1:p.His350Tyr
XM_024446266.1:c.2152C>T	XP_024302034.1:p.His718Tyr
XM_024446267.1:c.2152C>T	XP_024302035.1:p.His718Tyr
XM_024446268.1:c.2152C>T	XP_024302036.1:p.His718Tyr
XM_024446269.1:c.1072C>T	XP_024302037.1:p.His358Tyr
XR_001742362.1:n.2706C>T
NM_005460.4:c.2152C>T MANE Select	NP_005451.2:p.His718Tyr
NM_001308100.2:c.2293C>T	NP_001295029.1:p.His765Tyr
NM_001308107.2:c.1054C>T	NP_001295036.1:p.His352Tyr
NM_001308109.2:c.940C>T	NP_001295038.1:p.His314Tyr
NM_001242935.3:c.1054C>T	NP_001229864.1:p.His352Tyr