Canonical Allele Identifier: CA366255077

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535914T>A (hg19) ; chr6:g.158114882T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114882T>A , CM000668.2:g.158114882T>A	GRCh38
NC_000006.11:g.158535914T>A , CM000668.1:g.158535914T>A	GRCh37
NC_000006.10:g.158455902T>A	NCBI36
NG_032889.1:g.58399A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.803A>T	ENSP00000391168.2:n.803A>T
ENST00000607071.6:c.*1311A>T	ENSP00000475855.1:n.*1311A>T
ENST00000642244.1:c.1501A>T	ENSP00000493554.1:p.Ser501Cys
ENST00000642903.1:c.1591A>T	ENSP00000493559.1:p.Ser531Cys
ENST00000644972.1:c.1591A>T	ENSP00000496451.1:p.Ser531Cys
ENST00000645077.1:c.*1212A>T	ENSP00000496113.1:n.*1212A>T
ENST00000645172.1:c.*1293A>T	ENSP00000495367.1:n.*1293A>T
ENST00000646190.1:n.2922A>T
ENST00000646208.1:c.1327A>T	ENSP00000493723.1:p.Ser443Cys
ENST00000646410.1:c.1462A>T	ENSP00000494205.1:p.Ser488Cys
ENST00000646562.1:c.*1425A>T	ENSP00000496087.1:n.*1425A>T
ENST00000647468.2:c.1591A>T MANE Select	ENSP00000496731.1:p.Ser531Cys
ENST00000648111.1:c.*1279A>T	ENSP00000497275.1:n.*1279A>T
ENST00000367101.5:c.*39A>T	ENSP00000356068.1:n.*39A>T
ENST00000367104.7:c.1591A>T	ENSP00000356071.3:p.Ser531Cys
ENST00000435180.5:c.316A>T	ENSP00000391168.1:p.Ser106Cys
ENST00000606965.5:c.*152A>T	ENSP00000475808.1:n.*152A>T
ENST00000607071.5:c.*1525A>T	ENSP00000475855.1:n.*1525A>T
ENST00000607742.5:c.*2869A>T	ENSP00000475523.1:n.*2869A>T
NM_032861.3:c.1591A>T	NP_116250.3:p.Ser531Cys
NR_073096.1:n.1524A>T
XM_006715586.1:c.1381A>T	XP_006715649.1:p.Ser461Cys
XM_011536196.1:c.1570A>T	XP_011534498.1:p.Ser524Cys
XM_011536197.1:c.1477A>T	XP_011534499.1:p.Ser493Cys
XM_011536198.1:c.1381A>T	XP_011534500.1:p.Ser461Cys
XM_006715586.3:c.1381A>T	XP_006715649.1:p.Ser461Cys
XM_011536196.3:c.1570A>T	XP_011534498.1:p.Ser524Cys
XM_011536198.3:c.1381A>T	XP_011534500.1:p.Ser461Cys
XM_024446573.1:c.1591A>T	XP_024302341.1:p.Ser531Cys
XR_001743697.2:n.1622A>T
XR_942606.2:n.1673A>T
NM_032861.4:c.1591A>T MANE Select	NP_116250.3:p.Ser531Cys
NR_073096.2:n.1506A>T