Canonical Allele Identifier: CA387552175
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23358472A>G , CM000675.2:g.23358472A>G GRCh38
NC_000013.10:g.23932611A>G , CM000675.1:g.23932611A>G GRCh37
NC_000013.9:g.22830611A>G NCBI36
NG_012342.1:g.80231T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.467T>C ENSP00000508399.1:p.Leu156Pro
ENST00000682944.1:c.467T>C ENSP00000507173.1:p.Leu156Pro
ENST00000683154.1:n.605T>C
ENST00000683210.1:c.467T>C ENSP00000506739.1:p.Leu156Pro
ENST00000683270.1:c.458T>C ENSP00000507624.1:p.Leu153Pro
ENST00000683367.1:c.458T>C ENSP00000507780.1:p.Leu153Pro
ENST00000683489.1:c.467T>C ENSP00000508403.1:p.Leu156Pro
ENST00000683680.1:c.467T>C ENSP00000507223.1:p.Leu156Pro
ENST00000684163.1:c.458T>C ENSP00000508262.1:p.Leu153Pro
ENST00000684196.1:n.2824T>C
ENST00000684325.1:c.467T>C ENSP00000508121.1:p.Leu156Pro
ENST00000684385.1:c.467T>C ENSP00000507855.1:p.Leu156Pro
ENST00000684497.1:c.467T>C ENSP00000507057.1:p.Leu156Pro
ENST00000382292.9:c.467T>C MANE Select ENSP00000371729.3:p.Leu156Pro
ENST00000423156.2:c.467T>C ENSP00000390925.2:p.Leu156Pro
ENST00000455470.6:c.467T>C ENSP00000406565.2:p.Leu156Pro
ENST00000382292.7:c.467T>C ENSP00000371729.3:p.Leu156Pro
ENST00000382298.7:c.467T>C ENSP00000371735.3:p.Leu156Pro
ENST00000402364.1:c.-1784T>C ENSP00000385844.1:n.-1784T>C
ENST00000455470.5:c.165T>C
NM_001278055.1:c.26T>C NP_001264984.1:p.Leu9Pro
NM_014363.5:c.467T>C NP_055178.3:p.Leu156Pro
XM_005266338.1:c.467T>C XP_005266395.1:p.Leu156Pro
XM_011535038.1:c.491T>C XP_011533340.1:p.Leu164Pro
XM_011535039.1:c.458T>C XP_011533341.1:p.Leu153Pro
XM_005266338.2:c.467T>C XP_005266395.1:p.Leu156Pro
XM_011535039.2:c.458T>C XP_011533341.1:p.Leu153Pro
XM_017020539.1:c.458T>C XP_016876028.1:p.Leu153Pro
XM_024449337.1:c.467T>C XP_024305105.1:p.Leu156Pro
NM_014363.6:c.467T>C MANE Select NP_055178.3:p.Leu156Pro
NM_001278055.2:c.26T>C NP_001264984.1:p.Leu9Pro