Canonical Allele Identifier: CA387548846
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23355257G>C , CM000675.2:g.23355257G>C GRCh38
NC_000013.10:g.23929396G>C , CM000675.1:g.23929396G>C GRCh37
NC_000013.9:g.22827396G>C NCBI36
NG_012342.1:g.83446C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.1355C>G ENSP00000508399.1:p.Pro452Arg
ENST00000682944.1:c.1355C>G ENSP00000507173.1:p.Pro452Arg
ENST00000683154.1:n.1493C>G
ENST00000683210.1:c.1355C>G ENSP00000506739.1:p.Pro452Arg
ENST00000683270.1:c.1346C>G ENSP00000507624.1:p.Pro449Arg
ENST00000683367.1:c.1346C>G ENSP00000507780.1:p.Pro449Arg
ENST00000683489.1:c.1355C>G ENSP00000508403.1:p.Pro452Arg
ENST00000683680.1:c.1355C>G ENSP00000507223.1:p.Pro452Arg
ENST00000684163.1:c.1346C>G ENSP00000508262.1:p.Pro449Arg
ENST00000684196.1:n.3712C>G
ENST00000684325.1:c.1355C>G ENSP00000508121.1:p.Pro452Arg
ENST00000684385.1:c.1355C>G ENSP00000507855.1:p.Pro452Arg
ENST00000684497.1:c.1355C>G ENSP00000507057.1:p.Pro452Arg
ENST00000382292.9:c.1355C>G MANE Select ENSP00000371729.3:p.Pro452Arg
ENST00000423156.2:c.1355C>G ENSP00000390925.2:p.Pro452Arg
ENST00000455470.6:c.1355C>G ENSP00000406565.2:p.Pro452Arg
ENST00000382292.7:c.1355C>G ENSP00000371729.3:p.Pro452Arg
ENST00000382298.7:c.1355C>G ENSP00000371735.3:p.Pro452Arg
ENST00000402364.1:c.-896C>G ENSP00000385844.1:n.-896C>G
ENST00000423156.1:c.227C>G ENSP00000390925.1:p.Pro76Arg
ENST00000455470.5:c.1053C>G
NM_001278055.1:c.914C>G NP_001264984.1:p.Pro305Arg
NM_014363.5:c.1355C>G NP_055178.3:p.Pro452Arg
XM_005266338.1:c.1355C>G XP_005266395.1:p.Pro452Arg
XM_011535038.1:c.1379C>G XP_011533340.1:p.Pro460Arg
XM_011535039.1:c.1346C>G XP_011533341.1:p.Pro449Arg
XM_005266338.2:c.1355C>G XP_005266395.1:p.Pro452Arg
XM_011535039.2:c.1346C>G XP_011533341.1:p.Pro449Arg
XM_017020539.1:c.1346C>G XP_016876028.1:p.Pro449Arg
XM_024449337.1:c.1355C>G XP_024305105.1:p.Pro452Arg
NM_014363.6:c.1355C>G MANE Select NP_055178.3:p.Pro452Arg
NM_001278055.2:c.914C>G NP_001264984.1:p.Pro305Arg