Canonical Allele Identifier: CA366255240

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535979A>T (hg19) ; chr6:g.158114947A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114947A>T , CM000668.2:g.158114947A>T	GRCh38
NC_000006.11:g.158535979A>T , CM000668.1:g.158535979A>T	GRCh37
NC_000006.10:g.158455967A>T	NCBI36
NG_032889.1:g.58334T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.738T>A	ENSP00000391168.2:n.738T>A
ENST00000607071.6:c.*1246T>A	ENSP00000475855.1:n.*1246T>A
ENST00000642244.1:c.1436T>A	ENSP00000493554.1:p.Leu479Ter
ENST00000642903.1:c.1526T>A	ENSP00000493559.1:p.Leu509Ter
ENST00000644972.1:c.1526T>A	ENSP00000496451.1:p.Leu509Ter
ENST00000645077.1:c.*1147T>A	ENSP00000496113.1:n.*1147T>A
ENST00000645172.1:c.*1228T>A	ENSP00000495367.1:n.*1228T>A
ENST00000646190.1:n.2857T>A
ENST00000646208.1:c.1262T>A	ENSP00000493723.1:p.Leu421Ter
ENST00000646410.1:c.1397T>A	ENSP00000494205.1:p.Leu466Ter
ENST00000646562.1:c.*1360T>A	ENSP00000496087.1:n.*1360T>A
ENST00000647468.2:c.1526T>A MANE Select	ENSP00000496731.1:p.Leu509Ter
ENST00000648111.1:c.*1214T>A	ENSP00000497275.1:n.*1214T>A
ENST00000367101.5:c.1570T>A	ENSP00000356068.1:p.Trp524Arg
ENST00000367104.7:c.1526T>A	ENSP00000356071.3:p.Leu509Ter
ENST00000435180.5:c.251T>A	ENSP00000391168.1:p.Leu84Ter
ENST00000606965.5:c.*87T>A	ENSP00000475808.1:n.*87T>A
ENST00000607071.5:c.*1460T>A	ENSP00000475855.1:n.*1460T>A
ENST00000607742.5:c.*2804T>A	ENSP00000475523.1:n.*2804T>A
NM_032861.3:c.1526T>A	NP_116250.3:p.Leu509Ter
NR_073096.1:n.1459T>A
XM_006715586.1:c.1316T>A	XP_006715649.1:p.Leu439Ter
XM_011536196.1:c.1505T>A	XP_011534498.1:p.Leu502Ter
XM_011536197.1:c.1412T>A	XP_011534499.1:p.Leu471Ter
XM_011536198.1:c.1316T>A	XP_011534500.1:p.Leu439Ter
XM_006715586.3:c.1316T>A	XP_006715649.1:p.Leu439Ter
XM_011536196.3:c.1505T>A	XP_011534498.1:p.Leu502Ter
XM_011536198.3:c.1316T>A	XP_011534500.1:p.Leu439Ter
XM_024446573.1:c.1526T>A	XP_024302341.1:p.Leu509Ter
XR_001743697.2:n.1557T>A
XR_942606.2:n.1608T>A
NM_032861.4:c.1526T>A MANE Select	NP_116250.3:p.Leu509Ter
NR_073096.2:n.1441T>A