Canonical Allele Identifier: CA1675959402

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114843_158114845delinsCAG , CM000668.2:g.158114843_158114845delinsCAG	GRCh38
NC_000006.11:g.158535875_158535877delinsCAG , CM000668.1:g.158535875_158535877delinsCAG	GRCh37
NC_000006.10:g.158455863_158455865delinsCAG	NCBI36
NG_032889.1:g.58436_58438delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000435180.6:c.840_842delinsCTG	ENSP00000391168.2:n.840_842delinsCTG
ENST00000607071.6:c.*1348_*1350delinsCTG	ENSP00000475855.1:n.*1348_*1350delinsCTG
ENST00000642244.1:c.1538_1540delinsCTG	ENSP00000493554.1:p.Ser513=
ENST00000642903.1:c.1628_1630delinsCTG	ENSP00000493559.1:p.Ser543=
ENST00000644972.1:c.1628_1630delinsCTG	ENSP00000496451.1:p.Ser543=
ENST00000645077.1:c.*1249_*1251delinsCTG	ENSP00000496113.1:n.*1249_*1251delinsCTG
ENST00000645172.1:c.*1330_*1332delinsCTG	ENSP00000495367.1:n.*1330_*1332delinsCTG
ENST00000646190.1:n.2959_2961delinsCTG
ENST00000646208.1:c.1364_1366delinsCTG	ENSP00000493723.1:p.Ser455=
ENST00000646410.1:c.1499_1501delinsCTG	ENSP00000494205.1:p.Ser500=
ENST00000646562.1:c.*1462_*1464delinsCTG	ENSP00000496087.1:n.*1462_*1464delinsCTG
ENST00000647468.2:c.1628_1630delinsCTG MANE Select	ENSP00000496731.1:p.Ser543=
ENST00000648111.1:c.*1316_*1318delinsCTG	ENSP00000497275.1:n.*1316_*1318delinsCTG
ENST00000367101.5:c.*76_*78delinsCTG	ENSP00000356068.1:n.*76_*78delinsCTG
ENST00000367104.7:c.1628_1630delinsCTG	ENSP00000356071.3:p.Ser543=
ENST00000435180.5:c.353_355delinsCTG	ENSP00000391168.1:p.Ser118=
ENST00000606965.5:c.*189_*191delinsCTG	ENSP00000475808.1:n.*189_*191delinsCTG
ENST00000607071.5:c.*1562_*1564delinsCTG	ENSP00000475855.1:n.*1562_*1564delinsCTG
ENST00000607742.5:c.*2906_*2908delinsCTG	ENSP00000475523.1:n.*2906_*2908delinsCTG
NM_032861.3:c.1628_1630delinsCTG	NP_116250.3:p.Ser543=
NR_073096.1:n.1561_1563delinsCTG
XM_006715586.1:c.1418_1420delinsCTG	XP_006715649.1:p.Ser473=
XM_011536196.1:c.1607_1609delinsCTG	XP_011534498.1:p.Ser536=
XM_011536197.1:c.1514_1516delinsCTG	XP_011534499.1:p.Ser505=
XM_011536198.1:c.1418_1420delinsCTG	XP_011534500.1:p.Ser473=
XM_006715586.3:c.1418_1420delinsCTG	XP_006715649.1:p.Ser473=
XM_011536196.3:c.1607_1609delinsCTG	XP_011534498.1:p.Ser536=
XM_011536198.3:c.1418_1420delinsCTG	XP_011534500.1:p.Ser473=
XM_024446573.1:c.1628_1630delinsCTG	XP_024302341.1:p.Ser543=
XR_001743697.2:n.1659_1661delinsCTG
XR_942606.2:n.1710_1712delinsCTG
NM_032861.4:c.1628_1630delinsCTG MANE Select	NP_116250.3:p.Ser543=
NR_073096.2:n.1543_1545delinsCTG