Canonical Allele Identifier: CA2078621770
Gene: SACS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23334690_23334693delinsAAGG , CM000675.2:g.23334690_23334693delinsAAGG GRCh38
NC_000013.10:g.23908829_23908832delinsAAGG , CM000675.1:g.23908829_23908832delinsAAGG GRCh37
NC_000013.9:g.22806829_22806832delinsAAGG NCBI36
NG_012342.1:g.104010_104013delinsCCTT

Transcript Alleles

HGVS Amino-acid change
ENST00000682775.1:c.2185+19092_2185+19095delinsCCTT ENSP00000508399.1:n.2185+19092_2185+19095...
ENST00000682944.1:c.9210_9213delinsCCTT ENSP00000507173.1:p.Leu3070=
ENST00000683210.1:c.2185+19092_2185+19095delinsCCTT ENSP00000506739.1:n.2185+19092_2185+19095...
ENST00000683270.1:c.6445+2729_6445+2732delinsCCTT ENSP00000507624.1:n.6445+2729_6445+2732de...
ENST00000683367.1:c.2177-5209_2177-5206delinsCCTT ENSP00000507780.1:n.2177-5209_2177-5206de...
ENST00000683489.1:c.2292-4741_2292-4738delinsCCTT ENSP00000508403.1:n.2292-4741_2292-4738de...
ENST00000683680.1:c.2319-4741_2319-4738delinsCCTT ENSP00000507223.1:n.2319-4741_2319-4738de...
ENST00000684163.1:c.2204-5209_2204-5206delinsCCTT ENSP00000508262.1:n.2204-5209_2204-5206de...
ENST00000684196.1:n.4543-5209_4543-5206delinsCCTT
ENST00000684325.1:c.2186-13019_2186-13016delinsCCTT ENSP00000508121.1:n.2186-13019_2186-13016...
ENST00000684385.1:c.2221-5209_2221-5206delinsCCTT ENSP00000507855.1:n.2221-5209_2221-5206de...
ENST00000684497.1:c.2186-12049_2186-12046delinsCCTT ENSP00000507057.1:n.2186-12049_2186-12046...
ENST00000382292.9:c.9183_9186delinsCCTT MANE Select ENSP00000371729.3:p.Leu3061=
ENST00000423156.2:c.2186-5209_2186-5206delinsCCTT ENSP00000390925.2:n.2186-5209_2186-5206de...
ENST00000455470.6:c.2432-5209_2432-5206delinsCCTT ENSP00000406565.2:n.2432-5209_2432-5206de...
ENST00000382292.7:c.9183_9186delinsCCTT ENSP00000371729.3:p.Leu3061=
ENST00000382298.7:c.9183_9186delinsCCTT ENSP00000371735.3:p.Leu3061=
ENST00000402364.1:c.6933_6936delinsCCTT ENSP00000385844.1:p.Leu2311=
ENST00000423156.1:c.1058-5209_1058-5206delinsCCTT ENSP00000390925.1:n.1058-5209_1058-5206de...
ENST00000455470.5:c.2130-5209_2130-5206delinsCCTT
NM_001278055.1:c.8742_8745delinsCCTT NP_001264984.1:p.Leu2914=
NM_014363.5:c.9183_9186delinsCCTT NP_055178.3:p.Leu3061=
XM_005266338.1:c.9210_9213delinsCCTT XP_005266395.1:p.Leu3070=
XM_011535038.1:c.9234_9237delinsCCTT XP_011533340.1:p.Leu3078=
XM_011535039.1:c.9201_9204delinsCCTT XP_011533341.1:p.Leu3067=
XM_005266338.2:c.9210_9213delinsCCTT XP_005266395.1:p.Leu3070=
XM_011535039.2:c.9201_9204delinsCCTT XP_011533341.1:p.Leu3067=
XM_017020539.1:c.9174_9177delinsCCTT XP_016876028.1:p.Leu3058=
XM_024449337.1:c.9210_9213delinsCCTT XP_024305105.1:p.Leu3070=
NM_014363.6:c.9183_9186delinsCCTT MANE Select NP_055178.3:p.Leu3061=
NM_001278055.2:c.8742_8745delinsCCTT NP_001264984.1:p.Leu2914=