Canonical Allele Identifier: CA2578782250

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114914_158114916dup , CM000668.2:g.158114914_158114916dup	GRCh38
NC_000006.11:g.158535946_158535948dup , CM000668.1:g.158535946_158535948dup	GRCh37
NC_000006.10:g.158455934_158455936dup	NCBI36
NG_032889.1:g.58366_58368dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.770_772dup	ENSP00000391168.2:n.770_772dup
ENST00000607071.6:c.*1278_*1280dup	ENSP00000475855.1:n.*1278_*1280dup
ENST00000642244.1:c.1468_1470dup	ENSP00000493554.1:p.Val490_Ile491insVal
ENST00000642903.1:c.1558_1560dup	ENSP00000493559.1:p.Val520_Ile521insVal
ENST00000644972.1:c.1558_1560dup	ENSP00000496451.1:p.Val520_Ile521insVal
ENST00000645077.1:c.*1179_*1181dup	ENSP00000496113.1:n.*1179_*1181dup
ENST00000645172.1:c.*1260_*1262dup	ENSP00000495367.1:n.*1260_*1262dup
ENST00000646190.1:n.2889_2891dup
ENST00000646208.1:c.1294_1296dup	ENSP00000493723.1:p.Val432_Ile433insVal
ENST00000646410.1:c.1429_1431dup	ENSP00000494205.1:p.Val477_Ile478insVal
ENST00000646562.1:c.*1392_*1394dup	ENSP00000496087.1:n.*1392_*1394dup
ENST00000647468.2:c.1558_1560dup MANE Select	ENSP00000496731.1:p.Val520_Ile521insVal
ENST00000648111.1:c.*1246_*1248dup	ENSP00000497275.1:n.*1246_*1248dup
ENST00000367101.5:c.*6_*8dup	ENSP00000356068.1:n.*6_*8dup
ENST00000367104.7:c.1558_1560dup	ENSP00000356071.3:p.Val520_Ile521insVal
ENST00000435180.5:c.283_285dup	ENSP00000391168.1:p.Val95_Ile96insVal
ENST00000606965.5:c.*119_*121dup	ENSP00000475808.1:n.*119_*121dup
ENST00000607071.5:c.*1492_*1494dup	ENSP00000475855.1:n.*1492_*1494dup
ENST00000607742.5:c.*2836_*2838dup	ENSP00000475523.1:n.*2836_*2838dup
NM_032861.3:c.1558_1560dup	NP_116250.3:p.Val520_Ile521insVal
NR_073096.1:n.1491_1493dup
XM_006715586.1:c.1348_1350dup	XP_006715649.1:p.Val450_Ile451insVal
XM_011536196.1:c.1537_1539dup	XP_011534498.1:p.Val513_Ile514insVal
XM_011536197.1:c.1444_1446dup	XP_011534499.1:p.Val482_Ile483insVal
XM_011536198.1:c.1348_1350dup	XP_011534500.1:p.Val450_Ile451insVal
XM_006715586.3:c.1348_1350dup	XP_006715649.1:p.Val450_Ile451insVal
XM_011536196.3:c.1537_1539dup	XP_011534498.1:p.Val513_Ile514insVal
XM_011536198.3:c.1348_1350dup	XP_011534500.1:p.Val450_Ile451insVal
XM_024446573.1:c.1558_1560dup	XP_024302341.1:p.Val520_Ile521insVal
XR_001743697.2:n.1589_1591dup
XR_942606.2:n.1640_1642dup
NM_032861.4:c.1558_1560dup MANE Select	NP_116250.3:p.Val520_Ile521insVal
NR_073096.2:n.1473_1475dup