Canonical Allele Identifier: CA387513364
Gene: SACS HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.23908093G>A (hg19) chr13:g.23333954G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.23333954G>A , CM000675.2:g.23333954G>A GRCh38
NC_000013.10:g.23908093G>A , CM000675.1:g.23908093G>A GRCh37
NC_000013.9:g.22806093G>A NCBI36
NG_012342.1:g.104749C>T

Transcript Alleles

HGVS Amino-acid change
NM_001278055.1:c.9481C>T NP_001264984.1:p.His3161Tyr
NM_014363.5:c.9922C>T NP_055178.3:p.His3308Tyr
XM_005266338.1:c.9949C>T XP_005266395.1:p.His3317Tyr
XM_011535038.1:c.9973C>T XP_011533340.1:p.His3325Tyr
XM_011535039.1:c.9940C>T XP_011533341.1:p.His3314Tyr
XM_005266338.2:c.9949C>T XP_005266395.1:p.His3317Tyr
XM_011535039.2:c.9940C>T XP_011533341.1:p.His3314Tyr
XM_017020539.1:c.9913C>T XP_016876028.1:p.His3305Tyr
XM_024449337.1:c.9949C>T XP_024305105.1:p.His3317Tyr
NM_014363.6:c.9922C>T MANE Select NP_055178.3:p.His3308Tyr
NM_001278055.2:c.9481C>T NP_001264984.1:p.His3161Tyr
ENST00000382292.7:c.9922C>T ENSP00000371729.3:p.His3308Tyr
ENST00000382298.7:c.9922C>T ENSP00000371735.3:p.His3308Tyr
ENST00000402364.1:c.7672C>T ENSP00000385844.1:p.His2558Tyr
ENST00000423156.1:n.1058-4470C>T ENSP00000390925.1:p.=
ENST00000455470.5:n.2130-4470C>T
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