Canonical Allele Identifier: CA387506478
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330956A>G , CM000675.2:g.23330956A>G GRCh38
NC_000013.10:g.23905095A>G , CM000675.1:g.23905095A>G GRCh37
NC_000013.9:g.22803095A>G NCBI36
NG_012342.1:g.107747T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2186-18841T>C ENSP00000508399.1:n.2186-18841T>C
ENST00000682944.1:c.12947T>C ENSP00000507173.1:p.Leu4316Ser
ENST00000683210.1:c.2185+22829T>C ENSP00000506739.1:n.2185+22829T>C
ENST00000683270.1:c.6446-1472T>C ENSP00000507624.1:n.6446-1472T>C
ENST00000683367.1:c.2177-1472T>C ENSP00000507780.1:n.2177-1472T>C
ENST00000683489.1:c.2292-1004T>C ENSP00000508403.1:n.2292-1004T>C
ENST00000683680.1:c.2319-1004T>C ENSP00000507223.1:n.2319-1004T>C
ENST00000684163.1:c.2204-1472T>C ENSP00000508262.1:n.2204-1472T>C
ENST00000684196.1:n.4543-1472T>C
ENST00000684325.1:c.2186-9282T>C ENSP00000508121.1:n.2186-9282T>C
ENST00000684385.1:c.2221-1472T>C ENSP00000507855.1:n.2221-1472T>C
ENST00000684497.1:c.2186-8312T>C ENSP00000507057.1:n.2186-8312T>C
ENST00000382292.9:c.12920T>C MANE Select ENSP00000371729.3:p.Leu4307Ser
ENST00000423156.2:c.2186-1472T>C ENSP00000390925.2:n.2186-1472T>C
ENST00000455470.6:c.2432-1472T>C ENSP00000406565.2:n.2432-1472T>C
ENST00000382292.7:c.12920T>C ENSP00000371729.3:p.Leu4307Ser
ENST00000382298.7:c.12920T>C ENSP00000371735.3:p.Leu4307Ser
ENST00000402364.1:c.10670T>C ENSP00000385844.1:p.Leu3557Ser
ENST00000423156.1:c.1058-1472T>C ENSP00000390925.1:n.1058-1472T>C
ENST00000455470.5:c.2130-1472T>C
NM_001278055.1:c.12479T>C NP_001264984.1:p.Leu4160Ser
NM_014363.5:c.12920T>C NP_055178.3:p.Leu4307Ser
XM_005266338.1:c.12947T>C XP_005266395.1:p.Leu4316Ser
XM_011535038.1:c.12971T>C XP_011533340.1:p.Leu4324Ser
XM_011535039.1:c.12938T>C XP_011533341.1:p.Leu4313Ser
XM_005266338.2:c.12947T>C XP_005266395.1:p.Leu4316Ser
XM_011535039.2:c.12938T>C XP_011533341.1:p.Leu4313Ser
XM_017020539.1:c.12911T>C XP_016876028.1:p.Leu4304Ser
XM_024449337.1:c.12947T>C XP_024305105.1:p.Leu4316Ser
NM_014363.6:c.12920T>C MANE Select NP_055178.3:p.Leu4307Ser
NM_001278055.2:c.12479T>C NP_001264984.1:p.Leu4160Ser