Canonical Allele Identifier: CA387520553

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23911140A>G (hg19) ; chr13:g.23337001A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23337001A>G , CM000675.2:g.23337001A>G	GRCh38
NC_000013.10:g.23911140A>G , CM000675.1:g.23911140A>G	GRCh37
NC_000013.9:g.22809140A>G	NCBI36
NG_012342.1:g.101702T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682775.1:c.2185+16784T>C	ENSP00000508399.1:n.2185+16784T>C
ENST00000682944.1:c.6902T>C	ENSP00000507173.1:p.Leu2301Pro
ENST00000683210.1:c.2185+16784T>C	ENSP00000506739.1:n.2185+16784T>C
ENST00000683270.1:c.6445+421T>C	ENSP00000507624.1:n.6445+421T>C
ENST00000683367.1:c.2177-7517T>C	ENSP00000507780.1:n.2177-7517T>C
ENST00000683489.1:c.2291+4584T>C	ENSP00000508403.1:n.2291+4584T>C
ENST00000683680.1:c.2318+4584T>C	ENSP00000507223.1:n.2318+4584T>C
ENST00000684163.1:c.2204-7517T>C	ENSP00000508262.1:n.2204-7517T>C
ENST00000684196.1:n.4543-7517T>C
ENST00000684325.1:c.2186-15327T>C	ENSP00000508121.1:n.2186-15327T>C
ENST00000684385.1:c.2221-7517T>C	ENSP00000507855.1:n.2221-7517T>C
ENST00000684497.1:c.2186-14357T>C	ENSP00000507057.1:n.2186-14357T>C
ENST00000382292.9:c.6875T>C MANE Select	ENSP00000371729.3:p.Leu2292Pro
ENST00000423156.2:c.2186-7517T>C	ENSP00000390925.2:n.2186-7517T>C
ENST00000455470.6:c.2431+4444T>C	ENSP00000406565.2:n.2431+4444T>C
ENST00000382292.7:c.6875T>C	ENSP00000371729.3:p.Leu2292Pro
ENST00000382298.7:c.6875T>C	ENSP00000371735.3:p.Leu2292Pro
ENST00000402364.1:c.4625T>C	ENSP00000385844.1:p.Leu1542Pro
ENST00000423156.1:c.1058-7517T>C	ENSP00000390925.1:n.1058-7517T>C
ENST00000455470.5:c.2129+4444T>C
NM_001278055.1:c.6434T>C	NP_001264984.1:p.Leu2145Pro
NM_014363.5:c.6875T>C	NP_055178.3:p.Leu2292Pro
XM_005266338.1:c.6902T>C	XP_005266395.1:p.Leu2301Pro
XM_011535038.1:c.6926T>C	XP_011533340.1:p.Leu2309Pro
XM_011535039.1:c.6893T>C	XP_011533341.1:p.Leu2298Pro
XM_005266338.2:c.6902T>C	XP_005266395.1:p.Leu2301Pro
XM_011535039.2:c.6893T>C	XP_011533341.1:p.Leu2298Pro
XM_017020539.1:c.6866T>C	XP_016876028.1:p.Leu2289Pro
XM_024449337.1:c.6902T>C	XP_024305105.1:p.Leu2301Pro
NM_014363.6:c.6875T>C MANE Select	NP_055178.3:p.Leu2292Pro
NM_001278055.2:c.6434T>C	NP_001264984.1:p.Leu2145Pro