Canonical Allele Identifier: CA452820161

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535921A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114889A>T , CM000668.2:g.158114889A>T	GRCh38
NC_000006.11:g.158535921A>T , CM000668.1:g.158535921A>T	GRCh37
NC_000006.10:g.158455909A>T	NCBI36
NG_032889.1:g.58392T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.796T>A	ENSP00000391168.2:n.796T>A
ENST00000607071.6:c.*1304T>A	ENSP00000475855.1:n.*1304T>A
ENST00000642244.1:c.1494T>A	ENSP00000493554.1:p.Ile498=
ENST00000642903.1:c.1584T>A	ENSP00000493559.1:p.Ile528=
ENST00000644972.1:c.1584T>A	ENSP00000496451.1:p.Ile528=
ENST00000645077.1:c.*1205T>A	ENSP00000496113.1:n.*1205T>A
ENST00000645172.1:c.*1286T>A	ENSP00000495367.1:n.*1286T>A
ENST00000646190.1:n.2915T>A
ENST00000646208.1:c.1320T>A	ENSP00000493723.1:p.Ile440=
ENST00000646410.1:c.1455T>A	ENSP00000494205.1:p.Ile485=
ENST00000646562.1:c.*1418T>A	ENSP00000496087.1:n.*1418T>A
ENST00000647468.2:c.1584T>A MANE Select	ENSP00000496731.1:p.Ile528=
ENST00000648111.1:c.*1272T>A	ENSP00000497275.1:n.*1272T>A
ENST00000367101.5:c.*32T>A	ENSP00000356068.1:n.*32T>A
ENST00000367104.7:c.1584T>A	ENSP00000356071.3:p.Ile528=
ENST00000435180.5:c.309T>A	ENSP00000391168.1:p.Ile103=
ENST00000606965.5:c.*145T>A	ENSP00000475808.1:n.*145T>A
ENST00000607071.5:c.*1518T>A	ENSP00000475855.1:n.*1518T>A
ENST00000607742.5:c.*2862T>A	ENSP00000475523.1:n.*2862T>A
NM_032861.3:c.1584T>A	NP_116250.3:p.Ile528=
NR_073096.1:n.1517T>A
XM_006715586.1:c.1374T>A	XP_006715649.1:p.Ile458=
XM_011536196.1:c.1563T>A	XP_011534498.1:p.Ile521=
XM_011536197.1:c.1470T>A	XP_011534499.1:p.Ile490=
XM_011536198.1:c.1374T>A	XP_011534500.1:p.Ile458=
XM_006715586.3:c.1374T>A	XP_006715649.1:p.Ile458=
XM_011536196.3:c.1563T>A	XP_011534498.1:p.Ile521=
XM_011536198.3:c.1374T>A	XP_011534500.1:p.Ile458=
XM_024446573.1:c.1584T>A	XP_024302341.1:p.Ile528=
XR_001743697.2:n.1615T>A
XR_942606.2:n.1666T>A
NM_032861.4:c.1584T>A MANE Select	NP_116250.3:p.Ile528=
NR_073096.2:n.1499T>A