Canonical Allele Identifier: CA1975539251

Gene: SERPING1

Linked Data

• dbSNP Id: rs1945515727

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614476_57614477insTT , CM000673.2:g.57614476_57614477insTT	GRCh38
NC_000011.9:g.57381949_57381950insTT , CM000673.1:g.57381949_57381950insTT	GRCh37
NC_000011.8:g.57138525_57138526insTT	NCBI36
NG_009625.1:g.21923_21924insTT , LRG_105:g.21923_21924insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1398_1399insTT MANE Select	ENSP00000278407.4:p.Thr467LeufsTer?
ENST00000528996.2:c.*295_*296insTT	ENSP00000431226.2:n.*295_*296insTT
ENST00000531605.2:c.*1174_*1175insTT	ENSP00000503752.1:n.*1174_*1175insTT
ENST00000619430.2:c.1194_1195insTT	ENSP00000478572.2:p.Thr399LeufsTer?
ENST00000676670.1:c.1398_1399insTT	ENSP00000504807.1:p.Thr467LeufsTer?
ENST00000676741.1:n.2480_2481insTT
ENST00000677624.1:c.*818_*819insTT	ENSP00000503979.1:n.*818_*819insTT
ENST00000677625.1:c.1344_1345insTT	ENSP00000502857.1:p.Thr449LeufsTer?
ENST00000677856.1:n.1651_1652insTT
ENST00000677915.1:c.*295_*296insTT	ENSP00000503118.1:n.*295_*296insTT
ENST00000678533.1:c.*952_*953insTT	ENSP00000503873.1:n.*952_*953insTT
ENST00000678592.1:c.*338_*339insTT	ENSP00000504424.1:n.*338_*339insTT
ENST00000278407.8:c.1398_1399insTT	ENSP00000278407.4:p.Thr467LeufsTer?
ENST00000340687.10:c.1287_1288insTT	ENSP00000341861.6:p.Thr430LeufsTer?
ENST00000378323.8:c.1413_1414insTT	ENSP00000367574.4:p.Thr472LeufsTer?
ENST00000378324.6:c.1242_1243insTT	ENSP00000367575.2:p.Thr415LeufsTer?
ENST00000403558.1:c.1527_1528insTT	ENSP00000384420.1:p.Thr510LeufsTer?
ENST00000528996.1:c.599_600insTT	ENSP00000431226.1:n.599_600insTT
ENST00000530113.1:n.855_856insTT
ENST00000531133.5:c.899_900insTT	ENSP00000435431.1:n.899_900insTT
ENST00000531797.5:c.*423_*424insTT	ENSP00000432554.1:n.*423_*424insTT
ENST00000619430.1:c.529_530insTT	ENSP00000478572.1:n.529_530insTT
NM_000062.2:c.1398_1399insTT , LRG_105t1:c.1398_1399insTT	NP_000053.2:p.Thr467LeufsTer?
NM_001032295.1:c.1398_1399insTT	NP_001027466.1:p.Thr467LeufsTer?
NM_000062.3:c.1398_1399insTT MANE Select	NP_000053.2:p.Thr467LeufsTer?
NM_001032295.2:c.1398_1399insTT	NP_001027466.1:p.Thr467LeufsTer?