Canonical Allele Identifier: CA366255155

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535949G>A (hg19) ; chr6:g.158114917G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114917G>A , CM000668.2:g.158114917G>A	GRCh38
NC_000006.11:g.158535949G>A , CM000668.1:g.158535949G>A	GRCh37
NC_000006.10:g.158455937G>A	NCBI36
NG_032889.1:g.58364C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.768C>T	ENSP00000391168.2:n.768C>T
ENST00000607071.6:c.*1276C>T	ENSP00000475855.1:n.*1276C>T
ENST00000642244.1:c.1466C>T	ENSP00000493554.1:p.Thr489Ile
ENST00000642903.1:c.1556C>T	ENSP00000493559.1:p.Thr519Ile
ENST00000644972.1:c.1556C>T	ENSP00000496451.1:p.Thr519Ile
ENST00000645077.1:c.*1177C>T	ENSP00000496113.1:n.*1177C>T
ENST00000645172.1:c.*1258C>T	ENSP00000495367.1:n.*1258C>T
ENST00000646190.1:n.2887C>T
ENST00000646208.1:c.1292C>T	ENSP00000493723.1:p.Thr431Ile
ENST00000646410.1:c.1427C>T	ENSP00000494205.1:p.Thr476Ile
ENST00000646562.1:c.*1390C>T	ENSP00000496087.1:n.*1390C>T
ENST00000647468.2:c.1556C>T MANE Select	ENSP00000496731.1:p.Thr519Ile
ENST00000648111.1:c.*1244C>T	ENSP00000497275.1:n.*1244C>T
ENST00000367101.5:c.*4C>T	ENSP00000356068.1:n.*4C>T
ENST00000367104.7:c.1556C>T	ENSP00000356071.3:p.Thr519Ile
ENST00000435180.5:c.281C>T	ENSP00000391168.1:p.Thr94Ile
ENST00000606965.5:c.*117C>T	ENSP00000475808.1:n.*117C>T
ENST00000607071.5:c.*1490C>T	ENSP00000475855.1:n.*1490C>T
ENST00000607742.5:c.*2834C>T	ENSP00000475523.1:n.*2834C>T
NM_032861.3:c.1556C>T	NP_116250.3:p.Thr519Ile
NR_073096.1:n.1489C>T
XM_006715586.1:c.1346C>T	XP_006715649.1:p.Thr449Ile
XM_011536196.1:c.1535C>T	XP_011534498.1:p.Thr512Ile
XM_011536197.1:c.1442C>T	XP_011534499.1:p.Thr481Ile
XM_011536198.1:c.1346C>T	XP_011534500.1:p.Thr449Ile
XM_006715586.3:c.1346C>T	XP_006715649.1:p.Thr449Ile
XM_011536196.3:c.1535C>T	XP_011534498.1:p.Thr512Ile
XM_011536198.3:c.1346C>T	XP_011534500.1:p.Thr449Ile
XM_024446573.1:c.1556C>T	XP_024302341.1:p.Thr519Ile
XR_001743697.2:n.1587C>T
XR_942606.2:n.1638C>T
NM_032861.4:c.1556C>T MANE Select	NP_116250.3:p.Thr519Ile
NR_073096.2:n.1471C>T