Canonical Allele Identifier: CA366255055

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535903A>T (hg19) ; chr6:g.158114871A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114871A>T , CM000668.2:g.158114871A>T	GRCh38
NC_000006.11:g.158535903A>T , CM000668.1:g.158535903A>T	GRCh37
NC_000006.10:g.158455891A>T	NCBI36
NG_032889.1:g.58410T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.814T>A	ENSP00000391168.2:n.814T>A
ENST00000607071.6:c.*1322T>A	ENSP00000475855.1:n.*1322T>A
ENST00000642244.1:c.1512T>A	ENSP00000493554.1:p.His504Gln
ENST00000642903.1:c.1602T>A	ENSP00000493559.1:p.His534Gln
ENST00000644972.1:c.1602T>A	ENSP00000496451.1:p.His534Gln
ENST00000645077.1:c.*1223T>A	ENSP00000496113.1:n.*1223T>A
ENST00000645172.1:c.*1304T>A	ENSP00000495367.1:n.*1304T>A
ENST00000646190.1:n.2933T>A
ENST00000646208.1:c.1338T>A	ENSP00000493723.1:p.His446Gln
ENST00000646410.1:c.1473T>A	ENSP00000494205.1:p.His491Gln
ENST00000646562.1:c.*1436T>A	ENSP00000496087.1:n.*1436T>A
ENST00000647468.2:c.1602T>A MANE Select	ENSP00000496731.1:p.His534Gln
ENST00000648111.1:c.*1290T>A	ENSP00000497275.1:n.*1290T>A
ENST00000367101.5:c.*50T>A	ENSP00000356068.1:n.*50T>A
ENST00000367104.7:c.1602T>A	ENSP00000356071.3:p.His534Gln
ENST00000435180.5:c.327T>A	ENSP00000391168.1:p.His109Gln
ENST00000606965.5:c.*163T>A	ENSP00000475808.1:n.*163T>A
ENST00000607071.5:c.*1536T>A	ENSP00000475855.1:n.*1536T>A
ENST00000607742.5:c.*2880T>A	ENSP00000475523.1:n.*2880T>A
NM_032861.3:c.1602T>A	NP_116250.3:p.His534Gln
NR_073096.1:n.1535T>A
XM_006715586.1:c.1392T>A	XP_006715649.1:p.His464Gln
XM_011536196.1:c.1581T>A	XP_011534498.1:p.His527Gln
XM_011536197.1:c.1488T>A	XP_011534499.1:p.His496Gln
XM_011536198.1:c.1392T>A	XP_011534500.1:p.His464Gln
XM_006715586.3:c.1392T>A	XP_006715649.1:p.His464Gln
XM_011536196.3:c.1581T>A	XP_011534498.1:p.His527Gln
XM_011536198.3:c.1392T>A	XP_011534500.1:p.His464Gln
XM_024446573.1:c.1602T>A	XP_024302341.1:p.His534Gln
XR_001743697.2:n.1633T>A
XR_942606.2:n.1684T>A
NM_032861.4:c.1602T>A MANE Select	NP_116250.3:p.His534Gln
NR_073096.2:n.1517T>A