Canonical Allele Identifier: CA483159780

Gene: SACS

Linked Data

• gnomAD v4: 13-23334753-T-G
• MyVariant Identifiers: chr13:g.23908892T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.23334753T>G , CM000675.2:g.23334753T>G	GRCh38
NC_000013.10:g.23908892T>G , CM000675.1:g.23908892T>G	GRCh37
NC_000013.9:g.22806892T>G	NCBI36
NG_012342.1:g.103950A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682775.1:c.2185+19032A>C	ENSP00000508399.1:n.2185+19032A>C
ENST00000682944.1:c.9150A>C	ENSP00000507173.1:p.Ala3050=
ENST00000683210.1:c.2185+19032A>C	ENSP00000506739.1:n.2185+19032A>C
ENST00000683270.1:c.6445+2669A>C	ENSP00000507624.1:n.6445+2669A>C
ENST00000683367.1:c.2177-5269A>C	ENSP00000507780.1:n.2177-5269A>C
ENST00000683489.1:c.2292-4801A>C	ENSP00000508403.1:n.2292-4801A>C
ENST00000683680.1:c.2319-4801A>C	ENSP00000507223.1:n.2319-4801A>C
ENST00000684163.1:c.2204-5269A>C	ENSP00000508262.1:n.2204-5269A>C
ENST00000684196.1:n.4543-5269A>C
ENST00000684325.1:c.2186-13079A>C	ENSP00000508121.1:n.2186-13079A>C
ENST00000684385.1:c.2221-5269A>C	ENSP00000507855.1:n.2221-5269A>C
ENST00000684497.1:c.2186-12109A>C	ENSP00000507057.1:n.2186-12109A>C
ENST00000382292.9:c.9123A>C MANE Select	ENSP00000371729.3:p.Ala3041=
ENST00000423156.2:c.2186-5269A>C	ENSP00000390925.2:n.2186-5269A>C
ENST00000455470.6:c.2432-5269A>C	ENSP00000406565.2:n.2432-5269A>C
ENST00000382292.7:c.9123A>C	ENSP00000371729.3:p.Ala3041=
ENST00000382298.7:c.9123A>C	ENSP00000371735.3:p.Ala3041=
ENST00000402364.1:c.6873A>C	ENSP00000385844.1:p.Ala2291=
ENST00000423156.1:c.1058-5269A>C	ENSP00000390925.1:n.1058-5269A>C
ENST00000455470.5:c.2130-5269A>C
NM_001278055.1:c.8682A>C	NP_001264984.1:p.Ala2894=
NM_014363.5:c.9123A>C	NP_055178.3:p.Ala3041=
XM_005266338.1:c.9150A>C	XP_005266395.1:p.Ala3050=
XM_011535038.1:c.9174A>C	XP_011533340.1:p.Ala3058=
XM_011535039.1:c.9141A>C	XP_011533341.1:p.Ala3047=
XM_005266338.2:c.9150A>C	XP_005266395.1:p.Ala3050=
XM_011535039.2:c.9141A>C	XP_011533341.1:p.Ala3047=
XM_017020539.1:c.9114A>C	XP_016876028.1:p.Ala3038=
XM_024449337.1:c.9150A>C	XP_024305105.1:p.Ala3050=
NM_014363.6:c.9123A>C MANE Select	NP_055178.3:p.Ala3041=
NM_001278055.2:c.8682A>C	NP_001264984.1:p.Ala2894=