Canonical Allele Identifier: CA366264696

Gene: SERAC1

Linked Data

• dbSNP Id: rs2128421016
• MyVariant Identifiers: chr6:g.158567881G>T (hg19) ; chr6:g.158146849G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158146849G>T , CM000668.2:g.158146849G>T	GRCh38
NC_000006.11:g.158567881G>T , CM000668.1:g.158567881G>T	GRCh37
NC_000006.10:g.158487869G>T	NCBI36
NG_032889.1:g.26432C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*254C>A	ENSP00000475855.1:n.*254C>A
ENST00000642244.1:c.330C>A	ENSP00000493554.1:p.Ser110Arg
ENST00000642903.1:c.420C>A	ENSP00000493559.1:p.Ser140Arg
ENST00000644972.1:c.420C>A	ENSP00000496451.1:p.Ser140Arg
ENST00000645077.1:c.*254C>A	ENSP00000496113.1:n.*254C>A
ENST00000645172.1:c.*189+2016C>A	ENSP00000495367.1:n.*189+2016C>A
ENST00000646190.1:n.1651C>A
ENST00000646208.1:c.156C>A	ENSP00000493723.1:p.Ser52Arg
ENST00000646410.1:c.291C>A	ENSP00000494205.1:p.Ser97Arg
ENST00000646562.1:c.*254C>A	ENSP00000496087.1:n.*254C>A
ENST00000647468.2:c.420C>A MANE Select	ENSP00000496731.1:p.Ser140Arg
ENST00000648111.1:c.*64C>A	ENSP00000497275.1:n.*64C>A
ENST00000367101.5:c.420C>A	ENSP00000356068.1:p.Ser140Arg
ENST00000367104.7:c.420C>A	ENSP00000356071.3:p.Ser140Arg
ENST00000606965.5:c.420C>A	ENSP00000475808.1:p.Ser140Arg
ENST00000607000.1:c.420C>A	ENSP00000475788.1:p.Ser140Arg
ENST00000607071.5:c.*254C>A	ENSP00000475855.1:n.*254C>A
ENST00000607742.5:c.*254C>A	ENSP00000475523.1:n.*254C>A
NM_032861.3:c.420C>A	NP_116250.3:p.Ser140Arg
NR_073096.1:n.562C>A
XM_006715586.1:c.210C>A	XP_006715649.1:p.Ser70Arg
XM_011536196.1:c.399C>A	XP_011534498.1:p.Ser133Arg
XM_011536197.1:c.420C>A	XP_011534499.1:p.Ser140Arg
XM_011536198.1:c.210C>A	XP_011534500.1:p.Ser70Arg
XR_942606.1:n.421C>A
XM_006715586.3:c.210C>A	XP_006715649.1:p.Ser70Arg
XM_011536196.3:c.399C>A	XP_011534498.1:p.Ser133Arg
XM_011536198.3:c.210C>A	XP_011534500.1:p.Ser70Arg
XM_024446573.1:c.420C>A	XP_024302341.1:p.Ser140Arg
XR_001743697.2:n.501C>A
XR_942606.2:n.552C>A
NM_032861.4:c.420C>A MANE Select	NP_116250.3:p.Ser140Arg
NR_073096.2:n.544C>A