Canonical Allele Identifier: CA366254908

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535833C>G (hg19) ; chr6:g.158114801C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114801C>G , CM000668.2:g.158114801C>G	GRCh38
NC_000006.11:g.158535833C>G , CM000668.1:g.158535833C>G	GRCh37
NC_000006.10:g.158455821C>G	NCBI36
NG_032889.1:g.58480G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1392G>C	ENSP00000475855.1:n.*1392G>C
ENST00000642244.1:c.1582G>C	ENSP00000493554.1:p.Glu528Gln
ENST00000642903.1:c.1672G>C	ENSP00000493559.1:p.Glu558Gln
ENST00000644972.1:c.1672G>C	ENSP00000496451.1:p.Glu558Gln
ENST00000645077.1:c.*1293G>C	ENSP00000496113.1:n.*1293G>C
ENST00000645172.1:c.*1374G>C	ENSP00000495367.1:n.*1374G>C
ENST00000646190.1:n.3003G>C
ENST00000646208.1:c.1408G>C	ENSP00000493723.1:p.Glu470Gln
ENST00000646410.1:c.1543G>C	ENSP00000494205.1:p.Glu515Gln
ENST00000646562.1:c.*1506G>C	ENSP00000496087.1:n.*1506G>C
ENST00000647468.2:c.1672G>C MANE Select	ENSP00000496731.1:p.Glu558Gln
ENST00000648111.1:c.*1360G>C	ENSP00000497275.1:n.*1360G>C
ENST00000367101.5:c.*120G>C	ENSP00000356068.1:n.*120G>C
ENST00000367104.7:c.1672G>C	ENSP00000356071.3:p.Glu558Gln
ENST00000435180.5:c.397G>C	ENSP00000391168.1:p.Glu133Gln
ENST00000606965.5:c.*233G>C	ENSP00000475808.1:n.*233G>C
ENST00000607071.5:c.*1606G>C	ENSP00000475855.1:n.*1606G>C
ENST00000607742.5:c.*2950G>C	ENSP00000475523.1:n.*2950G>C
NM_032861.3:c.1672G>C	NP_116250.3:p.Glu558Gln
NR_073096.1:n.1605G>C
XM_006715586.1:c.1462G>C	XP_006715649.1:p.Glu488Gln
XM_011536196.1:c.1651G>C	XP_011534498.1:p.Glu551Gln
XM_011536197.1:c.1558G>C	XP_011534499.1:p.Glu520Gln
XM_011536198.1:c.1462G>C	XP_011534500.1:p.Glu488Gln
XM_006715586.3:c.1462G>C	XP_006715649.1:p.Glu488Gln
XM_011536196.3:c.1651G>C	XP_011534498.1:p.Glu551Gln
XM_011536198.3:c.1462G>C	XP_011534500.1:p.Glu488Gln
XM_024446573.1:c.1672G>C	XP_024302341.1:p.Glu558Gln
XR_001743697.2:n.1703G>C
XR_942606.2:n.1754G>C
NM_032861.4:c.1672G>C MANE Select	NP_116250.3:p.Glu558Gln
NR_073096.2:n.1587G>C