Canonical Allele Identifier: CA2680956606
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114716_158114717insTATAAAATGAGAGAATACATTCAAGGAA , CM000668.2:g.158114716_158114717insTATAAAATGAGAGAATACATTCAAGGAA GRCh38
NC_000006.11:g.158535748_158535749insTATAAAATGAGAGAATACATTCAAGGAA , CM000668.1:g.158535748_158535749insTATAAAATGAGAGAATACATTCAAGGAA GRCh37
NC_000006.10:g.158455736_158455737insTATAAAATGAGAGAATACATTCAAGGAA NCBI36
NG_032889.1:g.58579_58580insCTCTCATTTTATATTCCTTGAATGTATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+87_*1404+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000475855.1:n.*1404+87_*1404+88insCTCTCATTTTATATTCCTTGA...
ENST00000642244.1:c.1594+87_1594+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000493554.1:n.1594+87_1594+88insCTCTCATTTTATATTCCTTGAAT...
ENST00000642903.1:c.*7_*8insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000493559.1:n.*7_*8insCTCTCATTTTATATTCCTTGAATGTATT
ENST00000644972.1:c.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000496451.1:n.1684+87_1684+88insCTCTCATTTTATATTCCTTGAAT...
ENST00000645077.1:c.*1305+87_*1305+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000496113.1:n.*1305+87_*1305+88insCTCTCATTTTATATTCCTTGA...
ENST00000645172.1:c.*1386+87_*1386+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000495367.1:n.*1386+87_*1386+88insCTCTCATTTTATATTCCTTGA...
ENST00000646190.1:n.3015+87_3015+88insCTCTCATTTTATATTCCTTGAATGTATT
ENST00000646208.1:c.1420+87_1420+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000493723.1:n.1420+87_1420+88insCTCTCATTTTATATTCCTTGAAT...
ENST00000646410.1:c.1555+87_1555+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000494205.1:n.1555+87_1555+88insCTCTCATTTTATATTCCTTGAAT...
ENST00000646562.1:c.*1605_*1606insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000496087.1:n.*1605_*1606insCTCTCATTTTATATTCCTTGAATGTAT...
ENST00000647468.2:c.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT MANE Select ENSP00000496731.1:n.1684+87_1684+88insCTCTCATTTTATATTCCTTGAAT...
ENST00000648111.1:c.*1372+87_*1372+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000497275.1:n.*1372+87_*1372+88insCTCTCATTTTATATTCCTTGA...
ENST00000367104.7:c.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000356071.3:n.1684+87_1684+88insCTCTCATTTTATATTCCTTGAAT...
ENST00000435180.5:c.496_497insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000391168.1:n.496_497insCTCTCATTTTATATTCCTTGAATGTATT
ENST00000606965.5:c.*332_*333insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000475808.1:n.*332_*333insCTCTCATTTTATATTCCTTGAATGTATT
ENST00000607071.5:c.*1618+87_*1618+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000475855.1:n.*1618+87_*1618+88insCTCTCATTTTATATTCCTTGA...
ENST00000607742.5:c.*2962+87_*2962+88insCTCTCATTTTATATTCCTTGAATGTATT ENSP00000475523.1:n.*2962+87_*2962+88insCTCTCATTTTATATTCCTTGA...
NM_032861.3:c.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT NP_116250.3:n.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT
NR_073096.1:n.1704_1705insCTCTCATTTTATATTCCTTGAATGTATT
XM_006715586.1:c.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTATT XP_006715649.1:n.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTA...
XM_011536196.1:c.1663+87_1663+88insCTCTCATTTTATATTCCTTGAATGTATT XP_011534498.1:n.1663+87_1663+88insCTCTCATTTTATATTCCTTGAATGTA...
XM_011536197.1:c.1570+87_1570+88insCTCTCATTTTATATTCCTTGAATGTATT XP_011534499.1:n.1570+87_1570+88insCTCTCATTTTATATTCCTTGAATGTA...
XM_011536198.1:c.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTATT XP_011534500.1:n.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTA...
XM_006715586.3:c.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTATT XP_006715649.1:n.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTA...
XM_011536196.3:c.1663+87_1663+88insCTCTCATTTTATATTCCTTGAATGTATT XP_011534498.1:n.1663+87_1663+88insCTCTCATTTTATATTCCTTGAATGTA...
XM_011536198.3:c.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTATT XP_011534500.1:n.1474+87_1474+88insCTCTCATTTTATATTCCTTGAATGTA...
XM_024446573.1:c.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT XP_024302341.1:n.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTA...
XR_001743697.2:n.1715+87_1715+88insCTCTCATTTTATATTCCTTGAATGTATT
XR_942606.2:n.1766+87_1766+88insCTCTCATTTTATATTCCTTGAATGTATT
NM_032861.4:c.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT MANE Select NP_116250.3:n.1684+87_1684+88insCTCTCATTTTATATTCCTTGAATGTATT
NR_073096.2:n.1686_1687insCTCTCATTTTATATTCCTTGAATGTATT