Canonical Allele Identifier: CA2695207271

Gene: SERAC1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.158114831dup , CM000668.2:g.158114831dup	GRCh38
NC_000006.11:g.158535863dup , CM000668.1:g.158535863dup	GRCh37
NC_000006.10:g.158455851dup	NCBI36
NG_032889.1:g.58450dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000435180.6:c.854dup	ENSP00000391168.2:n.854dup
ENST00000607071.6:c.*1362dup	ENSP00000475855.1:n.*1362dup
ENST00000642244.1:c.1552dup	ENSP00000493554.1:p.Tyr518LeufsTer20
ENST00000642903.1:c.1642dup	ENSP00000493559.1:p.Tyr548LeufsTer16
ENST00000644972.1:c.1642dup	ENSP00000496451.1:p.Tyr548LeufsTer20
ENST00000645077.1:c.*1263dup	ENSP00000496113.1:n.*1263dup
ENST00000645172.1:c.*1344dup	ENSP00000495367.1:n.*1344dup
ENST00000646190.1:n.2973dup
ENST00000646208.1:c.1378dup	ENSP00000493723.1:p.Tyr460LeufsTer20
ENST00000646410.1:c.1513dup	ENSP00000494205.1:p.Tyr505LeufsTer20
ENST00000646562.1:c.*1476dup	ENSP00000496087.1:n.*1476dup
ENST00000647468.2:c.1642dup MANE Select	ENSP00000496731.1:p.Tyr548LeufsTer20
ENST00000648111.1:c.*1330dup	ENSP00000497275.1:n.*1330dup
ENST00000367101.5:c.*90dup	ENSP00000356068.1:n.*90dup
ENST00000367104.7:c.1642dup	ENSP00000356071.3:p.Tyr548LeufsTer20
ENST00000435180.5:c.367dup	ENSP00000391168.1:p.Tyr123LeufsTer16
ENST00000606965.5:c.*203dup	ENSP00000475808.1:n.*203dup
ENST00000607071.5:c.*1576dup	ENSP00000475855.1:n.*1576dup
ENST00000607742.5:c.*2920dup	ENSP00000475523.1:n.*2920dup
NM_032861.3:c.1642dup	NP_116250.3:p.Tyr548LeufsTer20
NR_073096.1:n.1575dup
XM_006715586.1:c.1432dup	XP_006715649.1:p.Tyr478LeufsTer20
XM_011536196.1:c.1621dup	XP_011534498.1:p.Tyr541LeufsTer20
XM_011536197.1:c.1528dup	XP_011534499.1:p.Tyr510LeufsTer20
XM_011536198.1:c.1432dup	XP_011534500.1:p.Tyr478LeufsTer20
XM_006715586.3:c.1432dup	XP_006715649.1:p.Tyr478LeufsTer20
XM_011536196.3:c.1621dup	XP_011534498.1:p.Tyr541LeufsTer20
XM_011536198.3:c.1432dup	XP_011534500.1:p.Tyr478LeufsTer20
XM_024446573.1:c.1642dup	XP_024302341.1:p.Tyr548LeufsTer20
XR_001743697.2:n.1673dup
XR_942606.2:n.1724dup
NM_032861.4:c.1642dup MANE Select	NP_116250.3:p.Tyr548LeufsTer20
NR_073096.2:n.1557dup