Canonical Allele Identifier: CA452820169

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535930T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114898T>C , CM000668.2:g.158114898T>C	GRCh38
NC_000006.11:g.158535930T>C , CM000668.1:g.158535930T>C	GRCh37
NC_000006.10:g.158455918T>C	NCBI36
NG_032889.1:g.58383A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.787A>G	ENSP00000391168.2:n.787A>G
ENST00000607071.6:c.*1295A>G	ENSP00000475855.1:n.*1295A>G
ENST00000642244.1:c.1485A>G	ENSP00000493554.1:p.Arg495=
ENST00000642903.1:c.1575A>G	ENSP00000493559.1:p.Arg525=
ENST00000644972.1:c.1575A>G	ENSP00000496451.1:p.Arg525=
ENST00000645077.1:c.*1196A>G	ENSP00000496113.1:n.*1196A>G
ENST00000645172.1:c.*1277A>G	ENSP00000495367.1:n.*1277A>G
ENST00000646190.1:n.2906A>G
ENST00000646208.1:c.1311A>G	ENSP00000493723.1:p.Arg437=
ENST00000646410.1:c.1446A>G	ENSP00000494205.1:p.Arg482=
ENST00000646562.1:c.*1409A>G	ENSP00000496087.1:n.*1409A>G
ENST00000647468.2:c.1575A>G MANE Select	ENSP00000496731.1:p.Arg525=
ENST00000648111.1:c.*1263A>G	ENSP00000497275.1:n.*1263A>G
ENST00000367101.5:c.*23A>G	ENSP00000356068.1:n.*23A>G
ENST00000367104.7:c.1575A>G	ENSP00000356071.3:p.Arg525=
ENST00000435180.5:c.300A>G	ENSP00000391168.1:p.Arg100=
ENST00000606965.5:c.*136A>G	ENSP00000475808.1:n.*136A>G
ENST00000607071.5:c.*1509A>G	ENSP00000475855.1:n.*1509A>G
ENST00000607742.5:c.*2853A>G	ENSP00000475523.1:n.*2853A>G
NM_032861.3:c.1575A>G	NP_116250.3:p.Arg525=
NR_073096.1:n.1508A>G
XM_006715586.1:c.1365A>G	XP_006715649.1:p.Arg455=
XM_011536196.1:c.1554A>G	XP_011534498.1:p.Arg518=
XM_011536197.1:c.1461A>G	XP_011534499.1:p.Arg487=
XM_011536198.1:c.1365A>G	XP_011534500.1:p.Arg455=
XM_006715586.3:c.1365A>G	XP_006715649.1:p.Arg455=
XM_011536196.3:c.1554A>G	XP_011534498.1:p.Arg518=
XM_011536198.3:c.1365A>G	XP_011534500.1:p.Arg455=
XM_024446573.1:c.1575A>G	XP_024302341.1:p.Arg525=
XR_001743697.2:n.1606A>G
XR_942606.2:n.1657A>G
NM_032861.4:c.1575A>G MANE Select	NP_116250.3:p.Arg525=
NR_073096.2:n.1490A>G