Canonical Allele Identifier: CA1675959020

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114563_158114569delinsATAATAT , CM000668.2:g.158114563_158114569delinsATAATAT	GRCh38
NC_000006.11:g.158535595_158535601delinsATAATAT , CM000668.1:g.158535595_158535601delinsATAATAT	GRCh37
NC_000006.10:g.158455583_158455589delinsATAATAT	NCBI36
NG_032889.1:g.58712_58718delinsATATTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+220_*1404+226delinsATATTAT	ENSP00000475855.1:n.*1404+220_*1404+226delinsATATTAT
ENST00000642244.1:c.1594+220_1594+226delinsATATTAT	ENSP00000493554.1:n.1594+220_1594+226delinsATATTAT
ENST00000644972.1:c.1684+220_1684+226delinsATATTAT	ENSP00000496451.1:n.1684+220_1684+226delinsATATTAT
ENST00000645077.1:c.*1305+220_*1305+226delinsATATTAT	ENSP00000496113.1:n.*1305+220_*1305+226delinsATATTAT
ENST00000645172.1:c.*1386+220_*1386+226delinsATATTAT	ENSP00000495367.1:n.*1386+220_*1386+226delinsATATTAT
ENST00000646190.1:n.3015+220_3015+226delinsATATTAT
ENST00000646208.1:c.1420+220_1420+226delinsATATTAT	ENSP00000493723.1:n.1420+220_1420+226delinsATATTAT
ENST00000646410.1:c.1555+220_1555+226delinsATATTAT	ENSP00000494205.1:n.1555+220_1555+226delinsATATTAT
ENST00000646562.1:c.*1738_*1744delinsATATTAT	ENSP00000496087.1:n.*1738_*1744delinsATATTAT
ENST00000647468.2:c.1684+220_1684+226delinsATATTAT MANE Select	ENSP00000496731.1:n.1684+220_1684+226delinsATATTAT
ENST00000648111.1:c.*1372+220_*1372+226delinsATATTAT	ENSP00000497275.1:n.*1372+220_*1372+226delinsATATTAT
ENST00000367104.7:c.1684+220_1684+226delinsATATTAT	ENSP00000356071.3:n.1684+220_1684+226delinsATATTAT
ENST00000606965.5:c.*465_*471delinsATATTAT	ENSP00000475808.1:n.*465_*471delinsATATTAT
ENST00000607071.5:c.*1618+220_*1618+226delinsATATTAT	ENSP00000475855.1:n.*1618+220_*1618+226delinsATATTAT
ENST00000607742.5:c.*2962+220_*2962+226delinsATATTAT	ENSP00000475523.1:n.*2962+220_*2962+226delinsATATTAT
NM_032861.3:c.1684+220_1684+226delinsATATTAT	NP_116250.3:n.1684+220_1684+226delinsATATTAT
NR_073096.1:n.1837_1843delinsATATTAT
XM_006715586.1:c.1474+220_1474+226delinsATATTAT	XP_006715649.1:n.1474+220_1474+226delinsATATTAT
XM_011536196.1:c.1663+220_1663+226delinsATATTAT	XP_011534498.1:n.1663+220_1663+226delinsATATTAT
XM_011536197.1:c.1570+220_1570+226delinsATATTAT	XP_011534499.1:n.1570+220_1570+226delinsATATTAT
XM_011536198.1:c.1474+220_1474+226delinsATATTAT	XP_011534500.1:n.1474+220_1474+226delinsATATTAT
XM_006715586.3:c.1474+220_1474+226delinsATATTAT	XP_006715649.1:n.1474+220_1474+226delinsATATTAT
XM_011536196.3:c.1663+220_1663+226delinsATATTAT	XP_011534498.1:n.1663+220_1663+226delinsATATTAT
XM_011536198.3:c.1474+220_1474+226delinsATATTAT	XP_011534500.1:n.1474+220_1474+226delinsATATTAT
XM_024446573.1:c.1684+220_1684+226delinsATATTAT	XP_024302341.1:n.1684+220_1684+226delinsATATTAT
XR_001743697.2:n.1715+220_1715+226delinsATATTAT
XR_942606.2:n.1766+220_1766+226delinsATATTAT
NM_032861.4:c.1684+220_1684+226delinsATATTAT MANE Select	NP_116250.3:n.1684+220_1684+226delinsATATTAT
NR_073096.2:n.1819_1825delinsATATTAT