Canonical Allele Identifier: CA387505533

Gene: SACS

Linked Data

• gnomAD v4: 13-23330563-A-C
• MyVariant Identifiers: chr13:g.23904702A>C (hg19) ; chr13:g.23330563A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23330563A>C , CM000675.2:g.23330563A>C	GRCh38
NC_000013.10:g.23904702A>C , CM000675.1:g.23904702A>C	GRCh37
NC_000013.9:g.22802702A>C	NCBI36
NG_012342.1:g.108140T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2186-18448T>G	ENSP00000508399.1:n.2186-18448T>G
ENST00000682944.1:c.13340T>G	ENSP00000507173.1:p.Phe4447Cys
ENST00000683210.1:c.2185+23222T>G	ENSP00000506739.1:n.2185+23222T>G
ENST00000683270.1:c.6446-1079T>G	ENSP00000507624.1:n.6446-1079T>G
ENST00000683367.1:c.2177-1079T>G	ENSP00000507780.1:n.2177-1079T>G
ENST00000683489.1:c.2292-611T>G	ENSP00000508403.1:n.2292-611T>G
ENST00000683680.1:c.2319-611T>G	ENSP00000507223.1:n.2319-611T>G
ENST00000684163.1:c.2204-1079T>G	ENSP00000508262.1:n.2204-1079T>G
ENST00000684196.1:n.4543-1079T>G
ENST00000684325.1:c.2186-8889T>G	ENSP00000508121.1:n.2186-8889T>G
ENST00000684385.1:c.2221-1079T>G	ENSP00000507855.1:n.2221-1079T>G
ENST00000684497.1:c.2186-7919T>G	ENSP00000507057.1:n.2186-7919T>G
ENST00000382292.9:c.13313T>G MANE Select	ENSP00000371729.3:p.Phe4438Cys
ENST00000423156.2:c.2186-1079T>G	ENSP00000390925.2:n.2186-1079T>G
ENST00000455470.6:c.2432-1079T>G	ENSP00000406565.2:n.2432-1079T>G
ENST00000382292.7:c.13313T>G	ENSP00000371729.3:p.Phe4438Cys
ENST00000382298.7:c.13313T>G	ENSP00000371735.3:p.Phe4438Cys
ENST00000402364.1:c.11063T>G	ENSP00000385844.1:p.Phe3688Cys
ENST00000423156.1:c.1058-1079T>G	ENSP00000390925.1:n.1058-1079T>G
ENST00000455470.5:c.2130-1079T>G
NM_001278055.1:c.12872T>G	NP_001264984.1:p.Phe4291Cys
NM_014363.5:c.13313T>G	NP_055178.3:p.Phe4438Cys
XM_005266338.1:c.13340T>G	XP_005266395.1:p.Phe4447Cys
XM_011535038.1:c.13364T>G	XP_011533340.1:p.Phe4455Cys
XM_011535039.1:c.13331T>G	XP_011533341.1:p.Phe4444Cys
XM_005266338.2:c.13340T>G	XP_005266395.1:p.Phe4447Cys
XM_011535039.2:c.13331T>G	XP_011533341.1:p.Phe4444Cys
XM_017020539.1:c.13304T>G	XP_016876028.1:p.Phe4435Cys
XM_024449337.1:c.13340T>G	XP_024305105.1:p.Phe4447Cys
NM_014363.6:c.13313T>G MANE Select	NP_055178.3:p.Phe4438Cys
NM_001278055.2:c.12872T>G	NP_001264984.1:p.Phe4291Cys