Canonical Allele Identifier: CA1675959032

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114569_158114572delinsTTAA , CM000668.2:g.158114569_158114572delinsTTAA	GRCh38
NC_000006.11:g.158535601_158535604delinsTTAA , CM000668.1:g.158535601_158535604delinsTTAA	GRCh37
NC_000006.10:g.158455589_158455592delinsTTAA	NCBI36
NG_032889.1:g.58709_58712delinsTTAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+217_*1404+220delinsTTAA	ENSP00000475855.1:n.*1404+217_*1404+220delinsTTAA
ENST00000642244.1:c.1594+217_1594+220delinsTTAA	ENSP00000493554.1:n.1594+217_1594+220delinsTTAA
ENST00000644972.1:c.1684+217_1684+220delinsTTAA	ENSP00000496451.1:n.1684+217_1684+220delinsTTAA
ENST00000645077.1:c.*1305+217_*1305+220delinsTTAA	ENSP00000496113.1:n.*1305+217_*1305+220delinsTTAA
ENST00000645172.1:c.*1386+217_*1386+220delinsTTAA	ENSP00000495367.1:n.*1386+217_*1386+220delinsTTAA
ENST00000646190.1:n.3015+217_3015+220delinsTTAA
ENST00000646208.1:c.1420+217_1420+220delinsTTAA	ENSP00000493723.1:n.1420+217_1420+220delinsTTAA
ENST00000646410.1:c.1555+217_1555+220delinsTTAA	ENSP00000494205.1:n.1555+217_1555+220delinsTTAA
ENST00000646562.1:c.*1735_*1738delinsTTAA	ENSP00000496087.1:n.*1735_*1738delinsTTAA
ENST00000647468.2:c.1684+217_1684+220delinsTTAA MANE Select	ENSP00000496731.1:n.1684+217_1684+220delinsTTAA
ENST00000648111.1:c.*1372+217_*1372+220delinsTTAA	ENSP00000497275.1:n.*1372+217_*1372+220delinsTTAA
ENST00000367104.7:c.1684+217_1684+220delinsTTAA	ENSP00000356071.3:n.1684+217_1684+220delinsTTAA
ENST00000606965.5:c.*462_*465delinsTTAA	ENSP00000475808.1:n.*462_*465delinsTTAA
ENST00000607071.5:c.*1618+217_*1618+220delinsTTAA	ENSP00000475855.1:n.*1618+217_*1618+220delinsTTAA
ENST00000607742.5:c.*2962+217_*2962+220delinsTTAA	ENSP00000475523.1:n.*2962+217_*2962+220delinsTTAA
NM_032861.3:c.1684+217_1684+220delinsTTAA	NP_116250.3:n.1684+217_1684+220delinsTTAA
NR_073096.1:n.1834_1837delinsTTAA
XM_006715586.1:c.1474+217_1474+220delinsTTAA	XP_006715649.1:n.1474+217_1474+220delinsTTAA
XM_011536196.1:c.1663+217_1663+220delinsTTAA	XP_011534498.1:n.1663+217_1663+220delinsTTAA
XM_011536197.1:c.1570+217_1570+220delinsTTAA	XP_011534499.1:n.1570+217_1570+220delinsTTAA
XM_011536198.1:c.1474+217_1474+220delinsTTAA	XP_011534500.1:n.1474+217_1474+220delinsTTAA
XM_006715586.3:c.1474+217_1474+220delinsTTAA	XP_006715649.1:n.1474+217_1474+220delinsTTAA
XM_011536196.3:c.1663+217_1663+220delinsTTAA	XP_011534498.1:n.1663+217_1663+220delinsTTAA
XM_011536198.3:c.1474+217_1474+220delinsTTAA	XP_011534500.1:n.1474+217_1474+220delinsTTAA
XM_024446573.1:c.1684+217_1684+220delinsTTAA	XP_024302341.1:n.1684+217_1684+220delinsTTAA
XR_001743697.2:n.1715+217_1715+220delinsTTAA
XR_942606.2:n.1766+217_1766+220delinsTTAA
NM_032861.4:c.1684+217_1684+220delinsTTAA MANE Select	NP_116250.3:n.1684+217_1684+220delinsTTAA
NR_073096.2:n.1816_1819delinsTTAA