Canonical Allele Identifier: CA452820122

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535891A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114859A>C , CM000668.2:g.158114859A>C	GRCh38
NC_000006.11:g.158535891A>C , CM000668.1:g.158535891A>C	GRCh37
NC_000006.10:g.158455879A>C	NCBI36
NG_032889.1:g.58422T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.826T>G	ENSP00000391168.2:n.826T>G
ENST00000607071.6:c.*1334T>G	ENSP00000475855.1:n.*1334T>G
ENST00000642244.1:c.1524T>G	ENSP00000493554.1:p.Arg508=
ENST00000642903.1:c.1614T>G	ENSP00000493559.1:p.Arg538=
ENST00000644972.1:c.1614T>G	ENSP00000496451.1:p.Arg538=
ENST00000645077.1:c.*1235T>G	ENSP00000496113.1:n.*1235T>G
ENST00000645172.1:c.*1316T>G	ENSP00000495367.1:n.*1316T>G
ENST00000646190.1:n.2945T>G
ENST00000646208.1:c.1350T>G	ENSP00000493723.1:p.Arg450=
ENST00000646410.1:c.1485T>G	ENSP00000494205.1:p.Arg495=
ENST00000646562.1:c.*1448T>G	ENSP00000496087.1:n.*1448T>G
ENST00000647468.2:c.1614T>G MANE Select	ENSP00000496731.1:p.Arg538=
ENST00000648111.1:c.*1302T>G	ENSP00000497275.1:n.*1302T>G
ENST00000367101.5:c.*62T>G	ENSP00000356068.1:n.*62T>G
ENST00000367104.7:c.1614T>G	ENSP00000356071.3:p.Arg538=
ENST00000435180.5:c.339T>G	ENSP00000391168.1:p.Arg113=
ENST00000606965.5:c.*175T>G	ENSP00000475808.1:n.*175T>G
ENST00000607071.5:c.*1548T>G	ENSP00000475855.1:n.*1548T>G
ENST00000607742.5:c.*2892T>G	ENSP00000475523.1:n.*2892T>G
NM_032861.3:c.1614T>G	NP_116250.3:p.Arg538=
NR_073096.1:n.1547T>G
XM_006715586.1:c.1404T>G	XP_006715649.1:p.Arg468=
XM_011536196.1:c.1593T>G	XP_011534498.1:p.Arg531=
XM_011536197.1:c.1500T>G	XP_011534499.1:p.Arg500=
XM_011536198.1:c.1404T>G	XP_011534500.1:p.Arg468=
XM_006715586.3:c.1404T>G	XP_006715649.1:p.Arg468=
XM_011536196.3:c.1593T>G	XP_011534498.1:p.Arg531=
XM_011536198.3:c.1404T>G	XP_011534500.1:p.Arg468=
XM_024446573.1:c.1614T>G	XP_024302341.1:p.Arg538=
XR_001743697.2:n.1645T>G
XR_942606.2:n.1696T>G
NM_032861.4:c.1614T>G MANE Select	NP_116250.3:p.Arg538=
NR_073096.2:n.1529T>G