Canonical Allele Identifier: CA366255139

Gene: SERAC1

Linked Data

• MyVariant Identifiers: chr6:g.158535940T>G (hg19) ; chr6:g.158114908T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114908T>G , CM000668.2:g.158114908T>G	GRCh38
NC_000006.11:g.158535940T>G , CM000668.1:g.158535940T>G	GRCh37
NC_000006.10:g.158455928T>G	NCBI36
NG_032889.1:g.58373A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.777A>C	ENSP00000391168.2:n.777A>C
ENST00000607071.6:c.*1285A>C	ENSP00000475855.1:n.*1285A>C
ENST00000642244.1:c.1475A>C	ENSP00000493554.1:p.Asn492Thr
ENST00000642903.1:c.1565A>C	ENSP00000493559.1:p.Asn522Thr
ENST00000644972.1:c.1565A>C	ENSP00000496451.1:p.Asn522Thr
ENST00000645077.1:c.*1186A>C	ENSP00000496113.1:n.*1186A>C
ENST00000645172.1:c.*1267A>C	ENSP00000495367.1:n.*1267A>C
ENST00000646190.1:n.2896A>C
ENST00000646208.1:c.1301A>C	ENSP00000493723.1:p.Asn434Thr
ENST00000646410.1:c.1436A>C	ENSP00000494205.1:p.Asn479Thr
ENST00000646562.1:c.*1399A>C	ENSP00000496087.1:n.*1399A>C
ENST00000647468.2:c.1565A>C MANE Select	ENSP00000496731.1:p.Asn522Thr
ENST00000648111.1:c.*1253A>C	ENSP00000497275.1:n.*1253A>C
ENST00000367101.5:c.*13A>C	ENSP00000356068.1:n.*13A>C
ENST00000367104.7:c.1565A>C	ENSP00000356071.3:p.Asn522Thr
ENST00000435180.5:c.290A>C	ENSP00000391168.1:p.Asn97Thr
ENST00000606965.5:c.*126A>C	ENSP00000475808.1:n.*126A>C
ENST00000607071.5:c.*1499A>C	ENSP00000475855.1:n.*1499A>C
ENST00000607742.5:c.*2843A>C	ENSP00000475523.1:n.*2843A>C
NM_032861.3:c.1565A>C	NP_116250.3:p.Asn522Thr
NR_073096.1:n.1498A>C
XM_006715586.1:c.1355A>C	XP_006715649.1:p.Asn452Thr
XM_011536196.1:c.1544A>C	XP_011534498.1:p.Asn515Thr
XM_011536197.1:c.1451A>C	XP_011534499.1:p.Asn484Thr
XM_011536198.1:c.1355A>C	XP_011534500.1:p.Asn452Thr
XM_006715586.3:c.1355A>C	XP_006715649.1:p.Asn452Thr
XM_011536196.3:c.1544A>C	XP_011534498.1:p.Asn515Thr
XM_011536198.3:c.1355A>C	XP_011534500.1:p.Asn452Thr
XM_024446573.1:c.1565A>C	XP_024302341.1:p.Asn522Thr
XR_001743697.2:n.1596A>C
XR_942606.2:n.1647A>C
NM_032861.4:c.1565A>C MANE Select	NP_116250.3:p.Asn522Thr
NR_073096.2:n.1480A>C