Canonical Allele Identifier: CA366255088

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535918A>T (hg19) ; chr6:g.158114886A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114886A>T , CM000668.2:g.158114886A>T	GRCh38
NC_000006.11:g.158535918A>T , CM000668.1:g.158535918A>T	GRCh37
NC_000006.10:g.158455906A>T	NCBI36
NG_032889.1:g.58395T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.799T>A	ENSP00000391168.2:n.799T>A
ENST00000607071.6:c.*1307T>A	ENSP00000475855.1:n.*1307T>A
ENST00000642244.1:c.1497T>A	ENSP00000493554.1:p.Phe499Leu
ENST00000642903.1:c.1587T>A	ENSP00000493559.1:p.Phe529Leu
ENST00000644972.1:c.1587T>A	ENSP00000496451.1:p.Phe529Leu
ENST00000645077.1:c.*1208T>A	ENSP00000496113.1:n.*1208T>A
ENST00000645172.1:c.*1289T>A	ENSP00000495367.1:n.*1289T>A
ENST00000646190.1:n.2918T>A
ENST00000646208.1:c.1323T>A	ENSP00000493723.1:p.Phe441Leu
ENST00000646410.1:c.1458T>A	ENSP00000494205.1:p.Phe486Leu
ENST00000646562.1:c.*1421T>A	ENSP00000496087.1:n.*1421T>A
ENST00000647468.2:c.1587T>A MANE Select	ENSP00000496731.1:p.Phe529Leu
ENST00000648111.1:c.*1275T>A	ENSP00000497275.1:n.*1275T>A
ENST00000367101.5:c.*35T>A	ENSP00000356068.1:n.*35T>A
ENST00000367104.7:c.1587T>A	ENSP00000356071.3:p.Phe529Leu
ENST00000435180.5:c.312T>A	ENSP00000391168.1:p.Phe104Leu
ENST00000606965.5:c.*148T>A	ENSP00000475808.1:n.*148T>A
ENST00000607071.5:c.*1521T>A	ENSP00000475855.1:n.*1521T>A
ENST00000607742.5:c.*2865T>A	ENSP00000475523.1:n.*2865T>A
NM_032861.3:c.1587T>A	NP_116250.3:p.Phe529Leu
NR_073096.1:n.1520T>A
XM_006715586.1:c.1377T>A	XP_006715649.1:p.Phe459Leu
XM_011536196.1:c.1566T>A	XP_011534498.1:p.Phe522Leu
XM_011536197.1:c.1473T>A	XP_011534499.1:p.Phe491Leu
XM_011536198.1:c.1377T>A	XP_011534500.1:p.Phe459Leu
XM_006715586.3:c.1377T>A	XP_006715649.1:p.Phe459Leu
XM_011536196.3:c.1566T>A	XP_011534498.1:p.Phe522Leu
XM_011536198.3:c.1377T>A	XP_011534500.1:p.Phe459Leu
XM_024446573.1:c.1587T>A	XP_024302341.1:p.Phe529Leu
XR_001743697.2:n.1618T>A
XR_942606.2:n.1669T>A
NM_032861.4:c.1587T>A MANE Select	NP_116250.3:p.Phe529Leu
NR_073096.2:n.1502T>A