Canonical Allele Identifier: CA2837240906

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611875_57611876delinsC , CM000673.2:g.57611875_57611876delinsC	GRCh38
NC_000011.9:g.57379348_57379349delinsC , CM000673.1:g.57379348_57379349delinsC	GRCh37
NC_000011.8:g.57135924_57135925delinsC	NCBI36
NG_009625.1:g.19322_19323delinsC , LRG_105:g.19322_19323delinsC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1188_1189delinsC MANE Select	ENSP00000278407.4:p.Thr397HisfsTer7
ENST00000528996.2:c.*85_*86delinsC	ENSP00000431226.2:n.*85_*86delinsC
ENST00000531605.2:c.*964_*965delinsC	ENSP00000503752.1:n.*964_*965delinsC
ENST00000619430.2:c.984_985delinsC	ENSP00000478572.2:p.Thr329HisfsTer7
ENST00000676670.1:c.1188_1189delinsC	ENSP00000504807.1:p.Thr397HisfsTer7
ENST00000676741.1:n.2270_2271delinsC
ENST00000677624.1:c.*608_*609delinsC	ENSP00000503979.1:n.*608_*609delinsC
ENST00000677625.1:c.1134_1135delinsC	ENSP00000502857.1:p.Thr379HisfsTer7
ENST00000677856.1:n.1441_1442delinsC
ENST00000677915.1:c.*85_*86delinsC	ENSP00000503118.1:n.*85_*86delinsC
ENST00000678533.1:c.*742_*743delinsC	ENSP00000503873.1:n.*742_*743delinsC
ENST00000678592.1:c.*128_*129delinsC	ENSP00000504424.1:n.*128_*129delinsC
ENST00000278407.8:c.1188_1189delinsC	ENSP00000278407.4:p.Thr397HisfsTer7
ENST00000340687.10:c.1077_1078delinsC	ENSP00000341861.6:p.Thr360HisfsTer7
ENST00000378323.8:c.1203_1204delinsC	ENSP00000367574.4:p.Thr402HisfsTer7
ENST00000378324.6:c.1032_1033delinsC	ENSP00000367575.2:p.Thr345HisfsTer7
ENST00000403558.1:c.1317_1318delinsC	ENSP00000384420.1:p.Thr440HisfsTer7
ENST00000528996.1:c.389_390delinsC	ENSP00000431226.1:n.389_390delinsC
ENST00000530113.1:n.645_646delinsC
ENST00000531133.5:c.689_690delinsC	ENSP00000435431.1:n.689_690delinsC
ENST00000531797.5:c.*213_*214delinsC	ENSP00000432554.1:n.*213_*214delinsC
ENST00000619430.1:c.349-30_349-29delinsC	ENSP00000478572.1:n.349-30_349-29delinsC
NM_000062.2:c.1188_1189delinsC , LRG_105t1:c.1188_1189delinsC	NP_000053.2:p.Thr397HisfsTer7
NM_001032295.1:c.1188_1189delinsC	NP_001027466.1:p.Thr397HisfsTer7
NM_000062.3:c.1188_1189delinsC MANE Select	NP_000053.2:p.Thr397HisfsTer7
NM_001032295.2:c.1188_1189delinsC	NP_001027466.1:p.Thr397HisfsTer7