Canonical Allele Identifier: CA452820106

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535876A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114844A>C , CM000668.2:g.158114844A>C	GRCh38
NC_000006.11:g.158535876A>C , CM000668.1:g.158535876A>C	GRCh37
NC_000006.10:g.158455864A>C	NCBI36
NG_032889.1:g.58437T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.841T>G	ENSP00000391168.2:n.841T>G
ENST00000607071.6:c.*1349T>G	ENSP00000475855.1:n.*1349T>G
ENST00000642244.1:c.1539T>G	ENSP00000493554.1:p.Ser513=
ENST00000642903.1:c.1629T>G	ENSP00000493559.1:p.Ser543=
ENST00000644972.1:c.1629T>G	ENSP00000496451.1:p.Ser543=
ENST00000645077.1:c.*1250T>G	ENSP00000496113.1:n.*1250T>G
ENST00000645172.1:c.*1331T>G	ENSP00000495367.1:n.*1331T>G
ENST00000646190.1:n.2960T>G
ENST00000646208.1:c.1365T>G	ENSP00000493723.1:p.Ser455=
ENST00000646410.1:c.1500T>G	ENSP00000494205.1:p.Ser500=
ENST00000646562.1:c.*1463T>G	ENSP00000496087.1:n.*1463T>G
ENST00000647468.2:c.1629T>G MANE Select	ENSP00000496731.1:p.Ser543=
ENST00000648111.1:c.*1317T>G	ENSP00000497275.1:n.*1317T>G
ENST00000367101.5:c.*77T>G	ENSP00000356068.1:n.*77T>G
ENST00000367104.7:c.1629T>G	ENSP00000356071.3:p.Ser543=
ENST00000435180.5:c.354T>G	ENSP00000391168.1:p.Ser118=
ENST00000606965.5:c.*190T>G	ENSP00000475808.1:n.*190T>G
ENST00000607071.5:c.*1563T>G	ENSP00000475855.1:n.*1563T>G
ENST00000607742.5:c.*2907T>G	ENSP00000475523.1:n.*2907T>G
NM_032861.3:c.1629T>G	NP_116250.3:p.Ser543=
NR_073096.1:n.1562T>G
XM_006715586.1:c.1419T>G	XP_006715649.1:p.Ser473=
XM_011536196.1:c.1608T>G	XP_011534498.1:p.Ser536=
XM_011536197.1:c.1515T>G	XP_011534499.1:p.Ser505=
XM_011536198.1:c.1419T>G	XP_011534500.1:p.Ser473=
XM_006715586.3:c.1419T>G	XP_006715649.1:p.Ser473=
XM_011536196.3:c.1608T>G	XP_011534498.1:p.Ser536=
XM_011536198.3:c.1419T>G	XP_011534500.1:p.Ser473=
XM_024446573.1:c.1629T>G	XP_024302341.1:p.Ser543=
XR_001743697.2:n.1660T>G
XR_942606.2:n.1711T>G
NM_032861.4:c.1629T>G MANE Select	NP_116250.3:p.Ser543=
NR_073096.2:n.1544T>G