Canonical Allele Identifier: CA452822191

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158567932T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146900T>A , CM000668.2:g.158146900T>A	GRCh38
NC_000006.11:g.158567932T>A , CM000668.1:g.158567932T>A	GRCh37
NC_000006.10:g.158487920T>A	NCBI36
NG_032889.1:g.26381A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*203A>T	ENSP00000475855.1:n.*203A>T
ENST00000642244.1:c.279A>T	ENSP00000493554.1:p.Thr93=
ENST00000642903.1:c.369A>T	ENSP00000493559.1:p.Thr123=
ENST00000643093.1:n.419A>T
ENST00000644972.1:c.369A>T	ENSP00000496451.1:p.Thr123=
ENST00000645077.1:c.*203A>T	ENSP00000496113.1:n.*203A>T
ENST00000645172.1:c.*189+1965A>T	ENSP00000495367.1:n.*189+1965A>T
ENST00000646190.1:n.1600A>T
ENST00000646208.1:c.105A>T	ENSP00000493723.1:p.Thr35=
ENST00000646410.1:c.240A>T	ENSP00000494205.1:p.Thr80=
ENST00000646562.1:c.*203A>T	ENSP00000496087.1:n.*203A>T
ENST00000647468.2:c.369A>T MANE Select	ENSP00000496731.1:p.Thr123=
ENST00000648111.1:c.*13A>T	ENSP00000497275.1:n.*13A>T
ENST00000367101.5:c.369A>T	ENSP00000356068.1:p.Thr123=
ENST00000367104.7:c.369A>T	ENSP00000356071.3:p.Thr123=
ENST00000606965.5:c.369A>T	ENSP00000475808.1:p.Thr123=
ENST00000607000.1:c.369A>T	ENSP00000475788.1:p.Thr123=
ENST00000607071.5:c.*203A>T	ENSP00000475855.1:n.*203A>T
ENST00000607742.5:c.*203A>T	ENSP00000475523.1:n.*203A>T
NM_032861.3:c.369A>T	NP_116250.3:p.Thr123=
NR_073096.1:n.511A>T
XM_006715586.1:c.159A>T	XP_006715649.1:p.Thr53=
XM_011536196.1:c.348A>T	XP_011534498.1:p.Thr116=
XM_011536197.1:c.369A>T	XP_011534499.1:p.Thr123=
XM_011536198.1:c.159A>T	XP_011534500.1:p.Thr53=
XR_942606.1:n.370A>T
XM_006715586.3:c.159A>T	XP_006715649.1:p.Thr53=
XM_011536196.3:c.348A>T	XP_011534498.1:p.Thr116=
XM_011536198.3:c.159A>T	XP_011534500.1:p.Thr53=
XM_024446573.1:c.369A>T	XP_024302341.1:p.Thr123=
XR_001743697.2:n.450A>T
XR_942606.2:n.501A>T
NM_032861.4:c.369A>T MANE Select	NP_116250.3:p.Thr123=
NR_073096.2:n.493A>T