Canonical Allele Identifier: CA452820067

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535831T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114799T>C , CM000668.2:g.158114799T>C	GRCh38
NC_000006.11:g.158535831T>C , CM000668.1:g.158535831T>C	GRCh37
NC_000006.10:g.158455819T>C	NCBI36
NG_032889.1:g.58482A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1394A>G	ENSP00000475855.1:n.*1394A>G
ENST00000642244.1:c.1584A>G	ENSP00000493554.1:p.Glu528=
ENST00000642903.1:c.1674A>G	ENSP00000493559.1:p.Glu558=
ENST00000644972.1:c.1674A>G	ENSP00000496451.1:p.Glu558=
ENST00000645077.1:c.*1295A>G	ENSP00000496113.1:n.*1295A>G
ENST00000645172.1:c.*1376A>G	ENSP00000495367.1:n.*1376A>G
ENST00000646190.1:n.3005A>G
ENST00000646208.1:c.1410A>G	ENSP00000493723.1:p.Glu470=
ENST00000646410.1:c.1545A>G	ENSP00000494205.1:p.Glu515=
ENST00000646562.1:c.*1508A>G	ENSP00000496087.1:n.*1508A>G
ENST00000647468.2:c.1674A>G MANE Select	ENSP00000496731.1:p.Glu558=
ENST00000648111.1:c.*1362A>G	ENSP00000497275.1:n.*1362A>G
ENST00000367101.5:c.*122A>G	ENSP00000356068.1:n.*122A>G
ENST00000367104.7:c.1674A>G	ENSP00000356071.3:p.Glu558=
ENST00000435180.5:c.399A>G	ENSP00000391168.1:p.Glu133=
ENST00000606965.5:c.*235A>G	ENSP00000475808.1:n.*235A>G
ENST00000607071.5:c.*1608A>G	ENSP00000475855.1:n.*1608A>G
ENST00000607742.5:c.*2952A>G	ENSP00000475523.1:n.*2952A>G
NM_032861.3:c.1674A>G	NP_116250.3:p.Glu558=
NR_073096.1:n.1607A>G
XM_006715586.1:c.1464A>G	XP_006715649.1:p.Glu488=
XM_011536196.1:c.1653A>G	XP_011534498.1:p.Glu551=
XM_011536197.1:c.1560A>G	XP_011534499.1:p.Glu520=
XM_011536198.1:c.1464A>G	XP_011534500.1:p.Glu488=
XM_006715586.3:c.1464A>G	XP_006715649.1:p.Glu488=
XM_011536196.3:c.1653A>G	XP_011534498.1:p.Glu551=
XM_011536198.3:c.1464A>G	XP_011534500.1:p.Glu488=
XM_024446573.1:c.1674A>G	XP_024302341.1:p.Glu558=
XR_001743697.2:n.1705A>G
XR_942606.2:n.1756A>G
NM_032861.4:c.1674A>G MANE Select	NP_116250.3:p.Glu558=
NR_073096.2:n.1589A>G