Canonical Allele Identifier: CA2773733419

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114890_158114891insCCAAACACACCCAACACA , CM000668.2:g.158114890_158114891insCCAAACACACCCAACACA	GRCh38
NC_000006.11:g.158535922_158535923insCCAAACACACCCAACACA , CM000668.1:g.158535922_158535923insCCAAACACACCCAACACA	GRCh37
NC_000006.10:g.158455910_158455911insCCAAACACACCCAACACA	NCBI36
NG_032889.1:g.58391_58392insGTGTTGGGTGTGTTTGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.795_796insGTGTTGGGTGTGTTTGGT	ENSP00000391168.2:n.795_796insGTGTTGGGTGTGTTTGGT
ENST00000607071.6:c.*1303_*1304insGTGTTGGGTGTGTTTGGT	ENSP00000475855.1:n.*1303_*1304insGTGTTGGGTGTGTTTGGT
ENST00000642244.1:c.1493_1494insGTGTTGGGTGTGTTTGGT	ENSP00000493554.1:p.Ile498delinsMetCysTrpValCysLeuVal
ENST00000642903.1:c.1583_1584insGTGTTGGGTGTGTTTGGT	ENSP00000493559.1:p.Ile528delinsMetCysTrpValCysLeuVal
ENST00000644972.1:c.1583_1584insGTGTTGGGTGTGTTTGGT	ENSP00000496451.1:p.Ile528delinsMetCysTrpValCysLeuVal
ENST00000645077.1:c.*1204_*1205insGTGTTGGGTGTGTTTGGT	ENSP00000496113.1:n.*1204_*1205insGTGTTGGGTGTGTTTGGT
ENST00000645172.1:c.*1285_*1286insGTGTTGGGTGTGTTTGGT	ENSP00000495367.1:n.*1285_*1286insGTGTTGGGTGTGTTTGGT
ENST00000646190.1:n.2914_2915insGTGTTGGGTGTGTTTGGT
ENST00000646208.1:c.1319_1320insGTGTTGGGTGTGTTTGGT	ENSP00000493723.1:p.Ile440delinsMetCysTrpValCysLeuVal
ENST00000646410.1:c.1454_1455insGTGTTGGGTGTGTTTGGT	ENSP00000494205.1:p.Ile485delinsMetCysTrpValCysLeuVal
ENST00000646562.1:c.*1417_*1418insGTGTTGGGTGTGTTTGGT	ENSP00000496087.1:n.*1417_*1418insGTGTTGGGTGTGTTTGGT
ENST00000647468.2:c.1583_1584insGTGTTGGGTGTGTTTGGT MANE Select	ENSP00000496731.1:p.Ile528delinsMetCysTrpValCysLeuVal
ENST00000648111.1:c.*1271_*1272insGTGTTGGGTGTGTTTGGT	ENSP00000497275.1:n.*1271_*1272insGTGTTGGGTGTGTTTGGT
ENST00000367101.5:c.*31_*32insGTGTTGGGTGTGTTTGGT	ENSP00000356068.1:n.*31_*32insGTGTTGGGTGTGTTTGGT
ENST00000367104.7:c.1583_1584insGTGTTGGGTGTGTTTGGT	ENSP00000356071.3:p.Ile528delinsMetCysTrpValCysLeuVal
ENST00000435180.5:c.308_309insGTGTTGGGTGTGTTTGGT	ENSP00000391168.1:p.Ile103delinsMetCysTrpValCysLeuVal
ENST00000606965.5:c.*144_*145insGTGTTGGGTGTGTTTGGT	ENSP00000475808.1:n.*144_*145insGTGTTGGGTGTGTTTGGT
ENST00000607071.5:c.*1517_*1518insGTGTTGGGTGTGTTTGGT	ENSP00000475855.1:n.*1517_*1518insGTGTTGGGTGTGTTTGGT
ENST00000607742.5:c.*2861_*2862insGTGTTGGGTGTGTTTGGT	ENSP00000475523.1:n.*2861_*2862insGTGTTGGGTGTGTTTGGT
NM_032861.3:c.1583_1584insGTGTTGGGTGTGTTTGGT	NP_116250.3:p.Ile528delinsMetCysTrpValCysLeuVal
NR_073096.1:n.1516_1517insGTGTTGGGTGTGTTTGGT
XM_006715586.1:c.1373_1374insGTGTTGGGTGTGTTTGGT	XP_006715649.1:p.Ile458delinsMetCysTrpValCysLeuVal
XM_011536196.1:c.1562_1563insGTGTTGGGTGTGTTTGGT	XP_011534498.1:p.Ile521delinsMetCysTrpValCysLeuVal
XM_011536197.1:c.1469_1470insGTGTTGGGTGTGTTTGGT	XP_011534499.1:p.Ile490delinsMetCysTrpValCysLeuVal
XM_011536198.1:c.1373_1374insGTGTTGGGTGTGTTTGGT	XP_011534500.1:p.Ile458delinsMetCysTrpValCysLeuVal
XM_006715586.3:c.1373_1374insGTGTTGGGTGTGTTTGGT	XP_006715649.1:p.Ile458delinsMetCysTrpValCysLeuVal
XM_011536196.3:c.1562_1563insGTGTTGGGTGTGTTTGGT	XP_011534498.1:p.Ile521delinsMetCysTrpValCysLeuVal
XM_011536198.3:c.1373_1374insGTGTTGGGTGTGTTTGGT	XP_011534500.1:p.Ile458delinsMetCysTrpValCysLeuVal
XM_024446573.1:c.1583_1584insGTGTTGGGTGTGTTTGGT	XP_024302341.1:p.Ile528delinsMetCysTrpValCysLeuVal
XR_001743697.2:n.1614_1615insGTGTTGGGTGTGTTTGGT
XR_942606.2:n.1665_1666insGTGTTGGGTGTGTTTGGT
NM_032861.4:c.1583_1584insGTGTTGGGTGTGTTTGGT MANE Select	NP_116250.3:p.Ile528delinsMetCysTrpValCysLeuVal
NR_073096.2:n.1498_1499insGTGTTGGGTGTGTTTGGT