Canonical Allele Identifier: CA366254959

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535857G>T (hg19) ; chr6:g.158114825G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114825G>T , CM000668.2:g.158114825G>T	GRCh38
NC_000006.11:g.158535857G>T , CM000668.1:g.158535857G>T	GRCh37
NC_000006.10:g.158455845G>T	NCBI36
NG_032889.1:g.58456C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1368C>A	ENSP00000475855.1:n.*1368C>A
ENST00000642244.1:c.1558C>A	ENSP00000493554.1:p.Leu520Ile
ENST00000642903.1:c.1648C>A	ENSP00000493559.1:p.Leu550Ile
ENST00000644972.1:c.1648C>A	ENSP00000496451.1:p.Leu550Ile
ENST00000645077.1:c.*1269C>A	ENSP00000496113.1:n.*1269C>A
ENST00000645172.1:c.*1350C>A	ENSP00000495367.1:n.*1350C>A
ENST00000646190.1:n.2979C>A
ENST00000646208.1:c.1384C>A	ENSP00000493723.1:p.Leu462Ile
ENST00000646410.1:c.1519C>A	ENSP00000494205.1:p.Leu507Ile
ENST00000646562.1:c.*1482C>A	ENSP00000496087.1:n.*1482C>A
ENST00000647468.2:c.1648C>A MANE Select	ENSP00000496731.1:p.Leu550Ile
ENST00000648111.1:c.*1336C>A	ENSP00000497275.1:n.*1336C>A
ENST00000367101.5:c.*96C>A	ENSP00000356068.1:n.*96C>A
ENST00000367104.7:c.1648C>A	ENSP00000356071.3:p.Leu550Ile
ENST00000435180.5:c.373C>A	ENSP00000391168.1:p.Leu125Ile
ENST00000606965.5:c.*209C>A	ENSP00000475808.1:n.*209C>A
ENST00000607071.5:c.*1582C>A	ENSP00000475855.1:n.*1582C>A
ENST00000607742.5:c.*2926C>A	ENSP00000475523.1:n.*2926C>A
NM_032861.3:c.1648C>A	NP_116250.3:p.Leu550Ile
NR_073096.1:n.1581C>A
XM_006715586.1:c.1438C>A	XP_006715649.1:p.Leu480Ile
XM_011536196.1:c.1627C>A	XP_011534498.1:p.Leu543Ile
XM_011536197.1:c.1534C>A	XP_011534499.1:p.Leu512Ile
XM_011536198.1:c.1438C>A	XP_011534500.1:p.Leu480Ile
XM_006715586.3:c.1438C>A	XP_006715649.1:p.Leu480Ile
XM_011536196.3:c.1627C>A	XP_011534498.1:p.Leu543Ile
XM_011536198.3:c.1438C>A	XP_011534500.1:p.Leu480Ile
XM_024446573.1:c.1648C>A	XP_024302341.1:p.Leu550Ile
XR_001743697.2:n.1679C>A
XR_942606.2:n.1730C>A
NM_032861.4:c.1648C>A MANE Select	NP_116250.3:p.Leu550Ile
NR_073096.2:n.1563C>A