Canonical Allele Identifier: CA387525819

Gene: SACS

Linked Data

• MyVariant Identifiers: chr13:g.23912644C>A (hg19) ; chr13:g.23338505C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23338505C>A , CM000675.2:g.23338505C>A	GRCh38
NC_000013.10:g.23912644C>A , CM000675.1:g.23912644C>A	GRCh37
NC_000013.9:g.22810644C>A	NCBI36
NG_012342.1:g.100198G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+15280G>T	ENSP00000508399.1:n.2185+15280G>T
ENST00000682944.1:c.5398G>T	ENSP00000507173.1:p.Ala1800Ser
ENST00000683210.1:c.2185+15280G>T	ENSP00000506739.1:n.2185+15280G>T
ENST00000683270.1:c.5362G>T	ENSP00000507624.1:p.Ala1788Ser
ENST00000683367.1:c.2177-9021G>T	ENSP00000507780.1:n.2177-9021G>T
ENST00000683489.1:c.2291+3080G>T	ENSP00000508403.1:n.2291+3080G>T
ENST00000683680.1:c.2318+3080G>T	ENSP00000507223.1:n.2318+3080G>T
ENST00000684163.1:c.2203+8306G>T	ENSP00000508262.1:n.2203+8306G>T
ENST00000684196.1:n.4543-9021G>T
ENST00000684325.1:c.2185+15280G>T	ENSP00000508121.1:n.2185+15280G>T
ENST00000684385.1:c.2220+8306G>T	ENSP00000507855.1:n.2220+8306G>T
ENST00000684497.1:c.2185+15280G>T	ENSP00000507057.1:n.2185+15280G>T
ENST00000382292.9:c.5371G>T MANE Select	ENSP00000371729.3:p.Ala1791Ser
ENST00000423156.2:c.2186-9021G>T	ENSP00000390925.2:n.2186-9021G>T
ENST00000455470.6:c.2431+2940G>T	ENSP00000406565.2:n.2431+2940G>T
ENST00000382292.7:c.5371G>T	ENSP00000371729.3:p.Ala1791Ser
ENST00000382298.7:c.5371G>T	ENSP00000371735.3:p.Ala1791Ser
ENST00000402364.1:c.3121G>T	ENSP00000385844.1:p.Ala1041Ser
ENST00000423156.1:c.1058-9021G>T	ENSP00000390925.1:n.1058-9021G>T
ENST00000455470.5:c.2129+2940G>T
NM_001278055.1:c.4930G>T	NP_001264984.1:p.Ala1644Ser
NM_014363.5:c.5371G>T	NP_055178.3:p.Ala1791Ser
XM_005266338.1:c.5398G>T	XP_005266395.1:p.Ala1800Ser
XM_011535038.1:c.5422G>T	XP_011533340.1:p.Ala1808Ser
XM_011535039.1:c.5389G>T	XP_011533341.1:p.Ala1797Ser
XM_005266338.2:c.5398G>T	XP_005266395.1:p.Ala1800Ser
XM_011535039.2:c.5389G>T	XP_011533341.1:p.Ala1797Ser
XM_017020539.1:c.5362G>T	XP_016876028.1:p.Ala1788Ser
XM_024449337.1:c.5398G>T	XP_024305105.1:p.Ala1800Ser
NM_014363.6:c.5371G>T MANE Select	NP_055178.3:p.Ala1791Ser
NM_001278055.2:c.4930G>T	NP_001264984.1:p.Ala1644Ser