Canonical Allele Identifier: CA2564994164
Gene: SERAC1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.158114720_158114721insTACATT , CM000668.2:g.158114720_158114721insTACATT GRCh38
NC_000006.11:g.158535752_158535753insTACATT , CM000668.1:g.158535752_158535753insTACATT GRCh37
NC_000006.10:g.158455740_158455741insTACATT NCBI36
NG_032889.1:g.58560_58561insAATGTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000607071.6:c.*1404+68_*1404+69insAATGTA ENSP00000475855.1:n.*1404+68_*1404+69insAATGTA
ENST00000642244.1:c.1594+68_1594+69insAATGTA ENSP00000493554.1:n.1594+68_1594+69insAATGTA
ENST00000642903.1:c.1752_1753insAATGTA ENSP00000493559.1:p.Lys584_Phe585insAsnVal
ENST00000644972.1:c.1684+68_1684+69insAATGTA ENSP00000496451.1:n.1684+68_1684+69insAATGTA
ENST00000645077.1:c.*1305+68_*1305+69insAATGTA ENSP00000496113.1:n.*1305+68_*1305+69insAATGTA
ENST00000645172.1:c.*1386+68_*1386+69insAATGTA ENSP00000495367.1:n.*1386+68_*1386+69insAATGTA
ENST00000646190.1:n.3015+68_3015+69insAATGTA
ENST00000646208.1:c.1420+68_1420+69insAATGTA ENSP00000493723.1:n.1420+68_1420+69insAATGTA
ENST00000646410.1:c.1555+68_1555+69insAATGTA ENSP00000494205.1:n.1555+68_1555+69insAATGTA
ENST00000646562.1:c.*1586_*1587insAATGTA ENSP00000496087.1:n.*1586_*1587insAATGTA
ENST00000647468.2:c.1684+68_1684+69insAATGTA MANE Select ENSP00000496731.1:n.1684+68_1684+69insAATGTA
ENST00000648111.1:c.*1372+68_*1372+69insAATGTA ENSP00000497275.1:n.*1372+68_*1372+69insAATGTA
ENST00000367104.7:c.1684+68_1684+69insAATGTA ENSP00000356071.3:n.1684+68_1684+69insAATGTA
ENST00000435180.5:c.477_478insAATGTA ENSP00000391168.1:p.Lys159_Phe160insAsnVal
ENST00000606965.5:c.*313_*314insAATGTA ENSP00000475808.1:n.*313_*314insAATGTA
ENST00000607071.5:c.*1618+68_*1618+69insAATGTA ENSP00000475855.1:n.*1618+68_*1618+69insAATGTA
ENST00000607742.5:c.*2962+68_*2962+69insAATGTA ENSP00000475523.1:n.*2962+68_*2962+69insAATGTA
NM_032861.3:c.1684+68_1684+69insAATGTA NP_116250.3:n.1684+68_1684+69insAATGTA
NR_073096.1:n.1685_1686insAATGTA
XM_006715586.1:c.1474+68_1474+69insAATGTA XP_006715649.1:n.1474+68_1474+69insAATGTA
XM_011536196.1:c.1663+68_1663+69insAATGTA XP_011534498.1:n.1663+68_1663+69insAATGTA
XM_011536197.1:c.1570+68_1570+69insAATGTA XP_011534499.1:n.1570+68_1570+69insAATGTA
XM_011536198.1:c.1474+68_1474+69insAATGTA XP_011534500.1:n.1474+68_1474+69insAATGTA
XM_006715586.3:c.1474+68_1474+69insAATGTA XP_006715649.1:n.1474+68_1474+69insAATGTA
XM_011536196.3:c.1663+68_1663+69insAATGTA XP_011534498.1:n.1663+68_1663+69insAATGTA
XM_011536198.3:c.1474+68_1474+69insAATGTA XP_011534500.1:n.1474+68_1474+69insAATGTA
XM_024446573.1:c.1684+68_1684+69insAATGTA XP_024302341.1:n.1684+68_1684+69insAATGTA
XR_001743697.2:n.1715+68_1715+69insAATGTA
XR_942606.2:n.1766+68_1766+69insAATGTA
NM_032861.4:c.1684+68_1684+69insAATGTA MANE Select NP_116250.3:n.1684+68_1684+69insAATGTA
NR_073096.2:n.1667_1668insAATGTA