Canonical Allele Identifier: CA483157803
Gene: SACS HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.23905115A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23330976A>C , CM000675.2:g.23330976A>C GRCh38
NC_000013.10:g.23905115A>C , CM000675.1:g.23905115A>C GRCh37
NC_000013.9:g.22803115A>C NCBI36
NG_012342.1:g.107727T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2186-18861T>G ENSP00000508399.1:n.2186-18861T>G
ENST00000682944.1:c.12927T>G ENSP00000507173.1:p.Val4309=
ENST00000683210.1:c.2185+22809T>G ENSP00000506739.1:n.2185+22809T>G
ENST00000683270.1:c.6446-1492T>G ENSP00000507624.1:n.6446-1492T>G
ENST00000683367.1:c.2177-1492T>G ENSP00000507780.1:n.2177-1492T>G
ENST00000683489.1:c.2292-1024T>G ENSP00000508403.1:n.2292-1024T>G
ENST00000683680.1:c.2319-1024T>G ENSP00000507223.1:n.2319-1024T>G
ENST00000684163.1:c.2204-1492T>G ENSP00000508262.1:n.2204-1492T>G
ENST00000684196.1:n.4543-1492T>G
ENST00000684325.1:c.2186-9302T>G ENSP00000508121.1:n.2186-9302T>G
ENST00000684385.1:c.2221-1492T>G ENSP00000507855.1:n.2221-1492T>G
ENST00000684497.1:c.2186-8332T>G ENSP00000507057.1:n.2186-8332T>G
ENST00000382292.9:c.12900T>G MANE Select ENSP00000371729.3:p.Val4300=
ENST00000423156.2:c.2186-1492T>G ENSP00000390925.2:n.2186-1492T>G
ENST00000455470.6:c.2432-1492T>G ENSP00000406565.2:n.2432-1492T>G
ENST00000382292.7:c.12900T>G ENSP00000371729.3:p.Val4300=
ENST00000382298.7:c.12900T>G ENSP00000371735.3:p.Val4300=
ENST00000402364.1:c.10650T>G ENSP00000385844.1:p.Val3550=
ENST00000423156.1:c.1058-1492T>G ENSP00000390925.1:n.1058-1492T>G
ENST00000455470.5:c.2130-1492T>G
NM_001278055.1:c.12459T>G NP_001264984.1:p.Val4153=
NM_014363.5:c.12900T>G NP_055178.3:p.Val4300=
XM_005266338.1:c.12927T>G XP_005266395.1:p.Val4309=
XM_011535038.1:c.12951T>G XP_011533340.1:p.Val4317=
XM_011535039.1:c.12918T>G XP_011533341.1:p.Val4306=
XM_005266338.2:c.12927T>G XP_005266395.1:p.Val4309=
XM_011535039.2:c.12918T>G XP_011533341.1:p.Val4306=
XM_017020539.1:c.12891T>G XP_016876028.1:p.Val4297=
XM_024449337.1:c.12927T>G XP_024305105.1:p.Val4309=
NM_014363.6:c.12900T>G MANE Select NP_055178.3:p.Val4300=
NM_001278055.2:c.12459T>G NP_001264984.1:p.Val4153=