Canonical Allele Identifier: CA2680956489

Gene: SERAC1

Linked Data

• gnomAD v4: 6-158114688-T-TTATAAACTGAGATAATACATTCAGAGAA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114694_158114695insCTGAGATAATACATTCAGAGAATATAAA , CM000668.2:g.158114694_158114695insCTGAGATAATACATTCAGAGAATATAAA	GRCh38
NC_000006.11:g.158535726_158535727insCTGAGATAATACATTCAGAGAATATAAA , CM000668.1:g.158535726_158535727insCTGAGATAATACATTCAGAGAATATAAA	GRCh37
NC_000006.10:g.158455714_158455715insCTGAGATAATACATTCAGAGAATATAAA	NCBI36
NG_032889.1:g.58592_58593insTTCTCTGAATGTATTATCTCAGTTTATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000607071.6:c.*1404+100_*1404+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000475855.1:n.*1404+100_*1404+101insTTCTCTGAATGTATTATCT...
ENST00000642244.1:c.1594+100_1594+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000493554.1:n.1594+100_1594+101insTTCTCTGAATGTATTATCTCA...
ENST00000642903.1:c.*20_*21insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000493559.1:n.*20_*21insTTCTCTGAATGTATTATCTCAGTTTATA
ENST00000644972.1:c.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000496451.1:n.1684+100_1684+101insTTCTCTGAATGTATTATCTCA...
ENST00000645077.1:c.*1305+100_*1305+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000496113.1:n.*1305+100_*1305+101insTTCTCTGAATGTATTATCT...
ENST00000645172.1:c.*1386+100_*1386+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000495367.1:n.*1386+100_*1386+101insTTCTCTGAATGTATTATCT...
ENST00000646190.1:n.3015+100_3015+101insTTCTCTGAATGTATTATCTCAGTTTATA
ENST00000646208.1:c.1420+100_1420+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000493723.1:n.1420+100_1420+101insTTCTCTGAATGTATTATCTCA...
ENST00000646410.1:c.1555+100_1555+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000494205.1:n.1555+100_1555+101insTTCTCTGAATGTATTATCTCA...
ENST00000646562.1:c.*1618_*1619insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000496087.1:n.*1618_*1619insTTCTCTGAATGTATTATCTCAGTTTAT...
ENST00000647468.2:c.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTATA MANE Select	ENSP00000496731.1:n.1684+100_1684+101insTTCTCTGAATGTATTATCTCA...
ENST00000648111.1:c.*1372+100_*1372+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000497275.1:n.*1372+100_*1372+101insTTCTCTGAATGTATTATCT...
ENST00000367104.7:c.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000356071.3:n.1684+100_1684+101insTTCTCTGAATGTATTATCTCA...
ENST00000606965.5:c.*345_*346insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000475808.1:n.*345_*346insTTCTCTGAATGTATTATCTCAGTTTATA
ENST00000607071.5:c.*1618+100_*1618+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000475855.1:n.*1618+100_*1618+101insTTCTCTGAATGTATTATCT...
ENST00000607742.5:c.*2962+100_*2962+101insTTCTCTGAATGTATTATCTCAGTTTATA	ENSP00000475523.1:n.*2962+100_*2962+101insTTCTCTGAATGTATTATCT...
NM_032861.3:c.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTATA	NP_116250.3:n.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTAT...
NR_073096.1:n.1717_1718insTTCTCTGAATGTATTATCTCAGTTTATA
XM_006715586.1:c.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_006715649.1:n.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTT...
XM_011536196.1:c.1663+100_1663+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_011534498.1:n.1663+100_1663+101insTTCTCTGAATGTATTATCTCAGTT...
XM_011536197.1:c.1570+100_1570+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_011534499.1:n.1570+100_1570+101insTTCTCTGAATGTATTATCTCAGTT...
XM_011536198.1:c.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_011534500.1:n.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTT...
XM_006715586.3:c.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_006715649.1:n.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTT...
XM_011536196.3:c.1663+100_1663+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_011534498.1:n.1663+100_1663+101insTTCTCTGAATGTATTATCTCAGTT...
XM_011536198.3:c.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_011534500.1:n.1474+100_1474+101insTTCTCTGAATGTATTATCTCAGTT...
XM_024446573.1:c.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTATA	XP_024302341.1:n.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTT...
XR_001743697.2:n.1715+100_1715+101insTTCTCTGAATGTATTATCTCAGTTTATA
XR_942606.2:n.1766+100_1766+101insTTCTCTGAATGTATTATCTCAGTTTATA
NM_032861.4:c.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTATA MANE Select	NP_116250.3:n.1684+100_1684+101insTTCTCTGAATGTATTATCTCAGTTTAT...
NR_073096.2:n.1699_1700insTTCTCTGAATGTATTATCTCAGTTTATA