Canonical Allele Identifier: CA483163739
Gene: SACS HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.23915222G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23341083G>A , CM000675.2:g.23341083G>A GRCh38
NC_000013.10:g.23915222G>A , CM000675.1:g.23915222G>A GRCh37
NC_000013.9:g.22813222G>A NCBI36
NG_012342.1:g.97620C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+12702C>T ENSP00000508399.1:n.2185+12702C>T
ENST00000682944.1:c.2820C>T ENSP00000507173.1:p.Asn940=
ENST00000683210.1:c.2185+12702C>T ENSP00000506739.1:n.2185+12702C>T
ENST00000683270.1:c.2784C>T ENSP00000507624.1:p.Asn928=
ENST00000683367.1:c.2177-11599C>T ENSP00000507780.1:n.2177-11599C>T
ENST00000683489.1:c.2291+502C>T ENSP00000508403.1:n.2291+502C>T
ENST00000683680.1:c.2318+502C>T ENSP00000507223.1:n.2318+502C>T
ENST00000684163.1:c.2203+5728C>T ENSP00000508262.1:n.2203+5728C>T
ENST00000684196.1:n.4543-11599C>T
ENST00000684325.1:c.2185+12702C>T ENSP00000508121.1:n.2185+12702C>T
ENST00000684385.1:c.2220+5728C>T ENSP00000507855.1:n.2220+5728C>T
ENST00000684497.1:c.2185+12702C>T ENSP00000507057.1:n.2185+12702C>T
ENST00000382292.9:c.2793C>T MANE Select ENSP00000371729.3:p.Asn931=
ENST00000423156.2:c.2186-11599C>T ENSP00000390925.2:n.2186-11599C>T
ENST00000455470.6:c.2431+362C>T ENSP00000406565.2:n.2431+362C>T
ENST00000382292.7:c.2793C>T ENSP00000371729.3:p.Asn931=
ENST00000382298.7:c.2793C>T ENSP00000371735.3:p.Asn931=
ENST00000402364.1:c.543C>T ENSP00000385844.1:p.Asn181=
ENST00000423156.1:c.1058-11599C>T ENSP00000390925.1:n.1058-11599C>T
ENST00000455470.5:c.2129+362C>T
NM_001278055.1:c.2352C>T NP_001264984.1:p.Asn784=
NM_014363.5:c.2793C>T NP_055178.3:p.Asn931=
XM_005266338.1:c.2820C>T XP_005266395.1:p.Asn940=
XM_011535038.1:c.2844C>T XP_011533340.1:p.Asn948=
XM_011535039.1:c.2811C>T XP_011533341.1:p.Asn937=
XM_005266338.2:c.2820C>T XP_005266395.1:p.Asn940=
XM_011535039.2:c.2811C>T XP_011533341.1:p.Asn937=
XM_017020539.1:c.2784C>T XP_016876028.1:p.Asn928=
XM_024449337.1:c.2820C>T XP_024305105.1:p.Asn940=
NM_014363.6:c.2793C>T MANE Select NP_055178.3:p.Asn931=
NM_001278055.2:c.2352C>T NP_001264984.1:p.Asn784=