Canonical Allele Identifier: CA452820116

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535885A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114853A>T , CM000668.2:g.158114853A>T	GRCh38
NC_000006.11:g.158535885A>T , CM000668.1:g.158535885A>T	GRCh37
NC_000006.10:g.158455873A>T	NCBI36
NG_032889.1:g.58428T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.832T>A	ENSP00000391168.2:n.832T>A
ENST00000607071.6:c.*1340T>A	ENSP00000475855.1:n.*1340T>A
ENST00000642244.1:c.1530T>A	ENSP00000493554.1:p.Ala510=
ENST00000642903.1:c.1620T>A	ENSP00000493559.1:p.Ala540=
ENST00000644972.1:c.1620T>A	ENSP00000496451.1:p.Ala540=
ENST00000645077.1:c.*1241T>A	ENSP00000496113.1:n.*1241T>A
ENST00000645172.1:c.*1322T>A	ENSP00000495367.1:n.*1322T>A
ENST00000646190.1:n.2951T>A
ENST00000646208.1:c.1356T>A	ENSP00000493723.1:p.Ala452=
ENST00000646410.1:c.1491T>A	ENSP00000494205.1:p.Ala497=
ENST00000646562.1:c.*1454T>A	ENSP00000496087.1:n.*1454T>A
ENST00000647468.2:c.1620T>A MANE Select	ENSP00000496731.1:p.Ala540=
ENST00000648111.1:c.*1308T>A	ENSP00000497275.1:n.*1308T>A
ENST00000367101.5:c.*68T>A	ENSP00000356068.1:n.*68T>A
ENST00000367104.7:c.1620T>A	ENSP00000356071.3:p.Ala540=
ENST00000435180.5:c.345T>A	ENSP00000391168.1:p.Ala115=
ENST00000606965.5:c.*181T>A	ENSP00000475808.1:n.*181T>A
ENST00000607071.5:c.*1554T>A	ENSP00000475855.1:n.*1554T>A
ENST00000607742.5:c.*2898T>A	ENSP00000475523.1:n.*2898T>A
NM_032861.3:c.1620T>A	NP_116250.3:p.Ala540=
NR_073096.1:n.1553T>A
XM_006715586.1:c.1410T>A	XP_006715649.1:p.Ala470=
XM_011536196.1:c.1599T>A	XP_011534498.1:p.Ala533=
XM_011536197.1:c.1506T>A	XP_011534499.1:p.Ala502=
XM_011536198.1:c.1410T>A	XP_011534500.1:p.Ala470=
XM_006715586.3:c.1410T>A	XP_006715649.1:p.Ala470=
XM_011536196.3:c.1599T>A	XP_011534498.1:p.Ala533=
XM_011536198.3:c.1410T>A	XP_011534500.1:p.Ala470=
XM_024446573.1:c.1620T>A	XP_024302341.1:p.Ala540=
XR_001743697.2:n.1651T>A
XR_942606.2:n.1702T>A
NM_032861.4:c.1620T>A MANE Select	NP_116250.3:p.Ala540=
NR_073096.2:n.1535T>A