Canonical Allele Identifier: CA954038619
Gene: SACS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23341780_23341781insCTTTTTT , CM000675.2:g.23341780_23341781insCTTTTTT GRCh38
NC_000013.10:g.23915919_23915920insCTTTTTT , CM000675.1:g.23915919_23915920insCTTTTTT GRCh37
NC_000013.9:g.22813919_22813920insCTTTTTT NCBI36
NG_012342.1:g.96922_96923insAAAAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000682775.1:c.2185+12004_2185+12005insAAAAAAG ENSP00000508399.1:n.2185+12004_2185+12005insAAAAAAG
ENST00000682944.1:c.2213-91_2213-90insAAAAAAG ENSP00000507173.1:n.2213-91_2213-90insAAAAAAG
ENST00000683210.1:c.2185+12004_2185+12005insAAAAAAG ENSP00000506739.1:n.2185+12004_2185+12005insAAAAAAG
ENST00000683270.1:c.2177-91_2177-90insAAAAAAG ENSP00000507624.1:n.2177-91_2177-90insAAAAAAG
ENST00000683367.1:c.2176+12004_2176+12005insAAAAAAG ENSP00000507780.1:n.2176+12004_2176+12005insAAAAAAG
ENST00000683489.1:c.2186-91_2186-90insAAAAAAG ENSP00000508403.1:n.2186-91_2186-90insAAAAAAG
ENST00000683680.1:c.2213-91_2213-90insAAAAAAG ENSP00000507223.1:n.2213-91_2213-90insAAAAAAG
ENST00000684163.1:c.2203+5030_2203+5031insAAAAAAG ENSP00000508262.1:n.2203+5030_2203+5031insAAAAAAG
ENST00000684196.1:n.4542+12004_4542+12005insAAAAAAG
ENST00000684325.1:c.2185+12004_2185+12005insAAAAAAG ENSP00000508121.1:n.2185+12004_2185+12005insAAAAAAG
ENST00000684385.1:c.2220+5030_2220+5031insAAAAAAG ENSP00000507855.1:n.2220+5030_2220+5031insAAAAAAG
ENST00000684497.1:c.2185+12004_2185+12005insAAAAAAG ENSP00000507057.1:n.2185+12004_2185+12005insAAAAAAG
ENST00000382292.9:c.2186-91_2186-90insAAAAAAG MANE Select ENSP00000371729.3:n.2186-91_2186-90insAAAAAAG
ENST00000423156.2:c.2185+12004_2185+12005insAAAAAAG ENSP00000390925.2:n.2185+12004_2185+12005insAAAAAAG
ENST00000455470.6:c.2186-91_2186-90insAAAAAAG ENSP00000406565.2:n.2186-91_2186-90insAAAAAAG
ENST00000382292.7:c.2186-91_2186-90insAAAAAAG ENSP00000371729.3:n.2186-91_2186-90insAAAAAAG
ENST00000382298.7:c.2186-91_2186-90insAAAAAAG ENSP00000371735.3:n.2186-91_2186-90insAAAAAAG
ENST00000402364.1:c.-65-91_-65-90insAAAAAAG ENSP00000385844.1:n.-65-91_-65-90insAAAAAAG
ENST00000423156.1:c.1057+12004_1057+12005insAAAAAAG ENSP00000390925.1:n.1057+12004_1057+12005insAAAAAAG
ENST00000455470.5:c.1884-91_1884-90insAAAAAAG
NM_001278055.1:c.1745-91_1745-90insAAAAAAG NP_001264984.1:n.1745-91_1745-90insAAAAAAG
NM_014363.5:c.2186-91_2186-90insAAAAAAG NP_055178.3:n.2186-91_2186-90insAAAAAAG
XM_005266338.1:c.2213-91_2213-90insAAAAAAG XP_005266395.1:n.2213-91_2213-90insAAAAAAG
XM_011535038.1:c.2237-91_2237-90insAAAAAAG XP_011533340.1:n.2237-91_2237-90insAAAAAAG
XM_011535039.1:c.2204-91_2204-90insAAAAAAG XP_011533341.1:n.2204-91_2204-90insAAAAAAG
XM_005266338.2:c.2213-91_2213-90insAAAAAAG XP_005266395.1:n.2213-91_2213-90insAAAAAAG
XM_011535039.2:c.2204-91_2204-90insAAAAAAG XP_011533341.1:n.2204-91_2204-90insAAAAAAG
XM_017020539.1:c.2177-91_2177-90insAAAAAAG XP_016876028.1:n.2177-91_2177-90insAAAAAAG
XM_024449337.1:c.2213-91_2213-90insAAAAAAG XP_024305105.1:n.2213-91_2213-90insAAAAAAG
NM_014363.6:c.2186-91_2186-90insAAAAAAG MANE Select NP_055178.3:n.2186-91_2186-90insAAAAAAG
NM_001278055.2:c.1745-91_1745-90insAAAAAAG NP_001264984.1:n.1745-91_1745-90insAAAAAAG