Canonical Allele Identifier: CA366254910

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535834T>G (hg19) ; chr6:g.158114802T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114802T>G , CM000668.2:g.158114802T>G	GRCh38
NC_000006.11:g.158535834T>G , CM000668.1:g.158535834T>G	GRCh37
NC_000006.10:g.158455822T>G	NCBI36
NG_032889.1:g.58479A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1391A>C	ENSP00000475855.1:n.*1391A>C
ENST00000642244.1:c.1581A>C	ENSP00000493554.1:p.Lys527Asn
ENST00000642903.1:c.1671A>C	ENSP00000493559.1:p.Lys557Asn
ENST00000644972.1:c.1671A>C	ENSP00000496451.1:p.Lys557Asn
ENST00000645077.1:c.*1292A>C	ENSP00000496113.1:n.*1292A>C
ENST00000645172.1:c.*1373A>C	ENSP00000495367.1:n.*1373A>C
ENST00000646190.1:n.3002A>C
ENST00000646208.1:c.1407A>C	ENSP00000493723.1:p.Lys469Asn
ENST00000646410.1:c.1542A>C	ENSP00000494205.1:p.Lys514Asn
ENST00000646562.1:c.*1505A>C	ENSP00000496087.1:n.*1505A>C
ENST00000647468.2:c.1671A>C MANE Select	ENSP00000496731.1:p.Lys557Asn
ENST00000648111.1:c.*1359A>C	ENSP00000497275.1:n.*1359A>C
ENST00000367101.5:c.*119A>C	ENSP00000356068.1:n.*119A>C
ENST00000367104.7:c.1671A>C	ENSP00000356071.3:p.Lys557Asn
ENST00000435180.5:c.396A>C	ENSP00000391168.1:p.Lys132Asn
ENST00000606965.5:c.*232A>C	ENSP00000475808.1:n.*232A>C
ENST00000607071.5:c.*1605A>C	ENSP00000475855.1:n.*1605A>C
ENST00000607742.5:c.*2949A>C	ENSP00000475523.1:n.*2949A>C
NM_032861.3:c.1671A>C	NP_116250.3:p.Lys557Asn
NR_073096.1:n.1604A>C
XM_006715586.1:c.1461A>C	XP_006715649.1:p.Lys487Asn
XM_011536196.1:c.1650A>C	XP_011534498.1:p.Lys550Asn
XM_011536197.1:c.1557A>C	XP_011534499.1:p.Lys519Asn
XM_011536198.1:c.1461A>C	XP_011534500.1:p.Lys487Asn
XM_006715586.3:c.1461A>C	XP_006715649.1:p.Lys487Asn
XM_011536196.3:c.1650A>C	XP_011534498.1:p.Lys550Asn
XM_011536198.3:c.1461A>C	XP_011534500.1:p.Lys487Asn
XM_024446573.1:c.1671A>C	XP_024302341.1:p.Lys557Asn
XR_001743697.2:n.1702A>C
XR_942606.2:n.1753A>C
NM_032861.4:c.1671A>C MANE Select	NP_116250.3:p.Lys557Asn
NR_073096.2:n.1586A>C