Canonical Allele Identifier: CA1675959496

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114963_158114966delinsCAAG , CM000668.2:g.158114963_158114966delinsCAAG	GRCh38
NC_000006.11:g.158535995_158535998delinsCAAG , CM000668.1:g.158535995_158535998delinsCAAG	GRCh37
NC_000006.10:g.158455983_158455986delinsCAAG	NCBI36
NG_032889.1:g.58315_58318delinsCTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.719_722delinsCTTG	ENSP00000391168.2:n.719_722delinsCTTG
ENST00000607071.6:c.*1227_*1230delinsCTTG	ENSP00000475855.1:n.*1227_*1230delinsCTTG
ENST00000642244.1:c.1417_1420delinsCTTG	ENSP00000493554.1:p.Leu473=
ENST00000642903.1:c.1507_1510delinsCTTG	ENSP00000493559.1:p.Leu503=
ENST00000644972.1:c.1507_1510delinsCTTG	ENSP00000496451.1:p.Leu503=
ENST00000645077.1:c.*1128_*1131delinsCTTG	ENSP00000496113.1:n.*1128_*1131delinsCTTG
ENST00000645172.1:c.*1209_*1212delinsCTTG	ENSP00000495367.1:n.*1209_*1212delinsCTTG
ENST00000646190.1:n.2838_2841delinsCTTG
ENST00000646208.1:c.1243_1246delinsCTTG	ENSP00000493723.1:p.Leu415=
ENST00000646410.1:c.1378_1381delinsCTTG	ENSP00000494205.1:p.Leu460=
ENST00000646562.1:c.*1341_*1344delinsCTTG	ENSP00000496087.1:n.*1341_*1344delinsCTTG
ENST00000647468.2:c.1507_1510delinsCTTG MANE Select	ENSP00000496731.1:p.Leu503=
ENST00000648111.1:c.*1195_*1198delinsCTTG	ENSP00000497275.1:n.*1195_*1198delinsCTTG
ENST00000367101.5:c.1551_1554delinsCTTG	ENSP00000356068.1:p.Phe517=
ENST00000367104.7:c.1507_1510delinsCTTG	ENSP00000356071.3:p.Leu503=
ENST00000435180.5:c.232_235delinsCTTG	ENSP00000391168.1:p.Leu78=
ENST00000606965.5:c.*68_*71delinsCTTG	ENSP00000475808.1:n.*68_*71delinsCTTG
ENST00000607071.5:c.*1441_*1444delinsCTTG	ENSP00000475855.1:n.*1441_*1444delinsCTTG
ENST00000607742.5:c.*2785_*2788delinsCTTG	ENSP00000475523.1:n.*2785_*2788delinsCTTG
NM_032861.3:c.1507_1510delinsCTTG	NP_116250.3:p.Leu503=
NR_073096.1:n.1440_1443delinsCTTG
XM_006715586.1:c.1297_1300delinsCTTG	XP_006715649.1:p.Leu433=
XM_011536196.1:c.1486_1489delinsCTTG	XP_011534498.1:p.Leu496=
XM_011536197.1:c.1393_1396delinsCTTG	XP_011534499.1:p.Leu465=
XM_011536198.1:c.1297_1300delinsCTTG	XP_011534500.1:p.Leu433=
XM_006715586.3:c.1297_1300delinsCTTG	XP_006715649.1:p.Leu433=
XM_011536196.3:c.1486_1489delinsCTTG	XP_011534498.1:p.Leu496=
XM_011536198.3:c.1297_1300delinsCTTG	XP_011534500.1:p.Leu433=
XM_024446573.1:c.1507_1510delinsCTTG	XP_024302341.1:p.Leu503=
XR_001743697.2:n.1538_1541delinsCTTG
XR_942606.2:n.1589_1592delinsCTTG
NM_032861.4:c.1507_1510delinsCTTG MANE Select	NP_116250.3:p.Leu503=
NR_073096.2:n.1422_1425delinsCTTG