Canonical Allele Identifier: CA366255090

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535919A>T (hg19) ; chr6:g.158114887A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114887A>T , CM000668.2:g.158114887A>T	GRCh38
NC_000006.11:g.158535919A>T , CM000668.1:g.158535919A>T	GRCh37
NC_000006.10:g.158455907A>T	NCBI36
NG_032889.1:g.58394T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.798T>A	ENSP00000391168.2:n.798T>A
ENST00000607071.6:c.*1306T>A	ENSP00000475855.1:n.*1306T>A
ENST00000642244.1:c.1496T>A	ENSP00000493554.1:p.Phe499Tyr
ENST00000642903.1:c.1586T>A	ENSP00000493559.1:p.Phe529Tyr
ENST00000644972.1:c.1586T>A	ENSP00000496451.1:p.Phe529Tyr
ENST00000645077.1:c.*1207T>A	ENSP00000496113.1:n.*1207T>A
ENST00000645172.1:c.*1288T>A	ENSP00000495367.1:n.*1288T>A
ENST00000646190.1:n.2917T>A
ENST00000646208.1:c.1322T>A	ENSP00000493723.1:p.Phe441Tyr
ENST00000646410.1:c.1457T>A	ENSP00000494205.1:p.Phe486Tyr
ENST00000646562.1:c.*1420T>A	ENSP00000496087.1:n.*1420T>A
ENST00000647468.2:c.1586T>A MANE Select	ENSP00000496731.1:p.Phe529Tyr
ENST00000648111.1:c.*1274T>A	ENSP00000497275.1:n.*1274T>A
ENST00000367101.5:c.*34T>A	ENSP00000356068.1:n.*34T>A
ENST00000367104.7:c.1586T>A	ENSP00000356071.3:p.Phe529Tyr
ENST00000435180.5:c.311T>A	ENSP00000391168.1:p.Phe104Tyr
ENST00000606965.5:c.*147T>A	ENSP00000475808.1:n.*147T>A
ENST00000607071.5:c.*1520T>A	ENSP00000475855.1:n.*1520T>A
ENST00000607742.5:c.*2864T>A	ENSP00000475523.1:n.*2864T>A
NM_032861.3:c.1586T>A	NP_116250.3:p.Phe529Tyr
NR_073096.1:n.1519T>A
XM_006715586.1:c.1376T>A	XP_006715649.1:p.Phe459Tyr
XM_011536196.1:c.1565T>A	XP_011534498.1:p.Phe522Tyr
XM_011536197.1:c.1472T>A	XP_011534499.1:p.Phe491Tyr
XM_011536198.1:c.1376T>A	XP_011534500.1:p.Phe459Tyr
XM_006715586.3:c.1376T>A	XP_006715649.1:p.Phe459Tyr
XM_011536196.3:c.1565T>A	XP_011534498.1:p.Phe522Tyr
XM_011536198.3:c.1376T>A	XP_011534500.1:p.Phe459Tyr
XM_024446573.1:c.1586T>A	XP_024302341.1:p.Phe529Tyr
XR_001743697.2:n.1617T>A
XR_942606.2:n.1668T>A
NM_032861.4:c.1586T>A MANE Select	NP_116250.3:p.Phe529Tyr
NR_073096.2:n.1501T>A