Canonical Allele Identifier: CA1675959470

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114915_158114917delinsCAG , CM000668.2:g.158114915_158114917delinsCAG	GRCh38
NC_000006.11:g.158535947_158535949delinsCAG , CM000668.1:g.158535947_158535949delinsCAG	GRCh37
NC_000006.10:g.158455935_158455937delinsCAG	NCBI36
NG_032889.1:g.58364_58366delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.768_770delinsCTG	ENSP00000391168.2:n.768_770delinsCTG
ENST00000607071.6:c.*1276_*1278delinsCTG	ENSP00000475855.1:n.*1276_*1278delinsCTG
ENST00000642244.1:c.1466_1468delinsCTG	ENSP00000493554.1:p.Thr489=
ENST00000642903.1:c.1556_1558delinsCTG	ENSP00000493559.1:p.Thr519=
ENST00000644972.1:c.1556_1558delinsCTG	ENSP00000496451.1:p.Thr519=
ENST00000645077.1:c.*1177_*1179delinsCTG	ENSP00000496113.1:n.*1177_*1179delinsCTG
ENST00000645172.1:c.*1258_*1260delinsCTG	ENSP00000495367.1:n.*1258_*1260delinsCTG
ENST00000646190.1:n.2887_2889delinsCTG
ENST00000646208.1:c.1292_1294delinsCTG	ENSP00000493723.1:p.Thr431=
ENST00000646410.1:c.1427_1429delinsCTG	ENSP00000494205.1:p.Thr476=
ENST00000646562.1:c.*1390_*1392delinsCTG	ENSP00000496087.1:n.*1390_*1392delinsCTG
ENST00000647468.2:c.1556_1558delinsCTG MANE Select	ENSP00000496731.1:p.Thr519=
ENST00000648111.1:c.*1244_*1246delinsCTG	ENSP00000497275.1:n.*1244_*1246delinsCTG
ENST00000367101.5:c.*4_*6delinsCTG	ENSP00000356068.1:n.*4_*6delinsCTG
ENST00000367104.7:c.1556_1558delinsCTG	ENSP00000356071.3:p.Thr519=
ENST00000435180.5:c.281_283delinsCTG	ENSP00000391168.1:p.Thr94=
ENST00000606965.5:c.*117_*119delinsCTG	ENSP00000475808.1:n.*117_*119delinsCTG
ENST00000607071.5:c.*1490_*1492delinsCTG	ENSP00000475855.1:n.*1490_*1492delinsCTG
ENST00000607742.5:c.*2834_*2836delinsCTG	ENSP00000475523.1:n.*2834_*2836delinsCTG
NM_032861.3:c.1556_1558delinsCTG	NP_116250.3:p.Thr519=
NR_073096.1:n.1489_1491delinsCTG
XM_006715586.1:c.1346_1348delinsCTG	XP_006715649.1:p.Thr449=
XM_011536196.1:c.1535_1537delinsCTG	XP_011534498.1:p.Thr512=
XM_011536197.1:c.1442_1444delinsCTG	XP_011534499.1:p.Thr481=
XM_011536198.1:c.1346_1348delinsCTG	XP_011534500.1:p.Thr449=
XM_006715586.3:c.1346_1348delinsCTG	XP_006715649.1:p.Thr449=
XM_011536196.3:c.1535_1537delinsCTG	XP_011534498.1:p.Thr512=
XM_011536198.3:c.1346_1348delinsCTG	XP_011534500.1:p.Thr449=
XM_024446573.1:c.1556_1558delinsCTG	XP_024302341.1:p.Thr519=
XR_001743697.2:n.1587_1589delinsCTG
XR_942606.2:n.1638_1640delinsCTG
NM_032861.4:c.1556_1558delinsCTG MANE Select	NP_116250.3:p.Thr519=
NR_073096.2:n.1471_1473delinsCTG