Canonical Allele Identifier: CA1975539269

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614486_57614487delinsGT , CM000673.2:g.57614486_57614487delinsGT	GRCh38
NC_000011.9:g.57381959_57381960delinsGT , CM000673.1:g.57381959_57381960delinsGT	GRCh37
NC_000011.8:g.57138535_57138536delinsGT	NCBI36
NG_009625.1:g.21933_21934delinsGT , LRG_105:g.21933_21934delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1408_1409delinsGT MANE Select	ENSP00000278407.4:p.Val470=
ENST00000528996.2:c.*305_*306delinsGT	ENSP00000431226.2:n.*305_*306delinsGT
ENST00000531605.2:c.*1184_*1185delinsGT	ENSP00000503752.1:n.*1184_*1185delinsGT
ENST00000619430.2:c.1204_1205delinsGT	ENSP00000478572.2:p.Val402=
ENST00000676670.1:c.1408_1409delinsGT	ENSP00000504807.1:p.Val470=
ENST00000676741.1:n.2490_2491delinsGT
ENST00000677624.1:c.*828_*829delinsGT	ENSP00000503979.1:n.*828_*829delinsGT
ENST00000677625.1:c.1354_1355delinsGT	ENSP00000502857.1:p.Val452=
ENST00000677856.1:n.1661_1662delinsGT
ENST00000677915.1:c.*305_*306delinsGT	ENSP00000503118.1:n.*305_*306delinsGT
ENST00000678533.1:c.*962_*963delinsGT	ENSP00000503873.1:n.*962_*963delinsGT
ENST00000678592.1:c.*348_*349delinsGT	ENSP00000504424.1:n.*348_*349delinsGT
ENST00000278407.8:c.1408_1409delinsGT	ENSP00000278407.4:p.Val470=
ENST00000340687.10:c.1297_1298delinsGT	ENSP00000341861.6:p.Val433=
ENST00000378323.8:c.1423_1424delinsGT	ENSP00000367574.4:p.Val475=
ENST00000378324.6:c.1252_1253delinsGT	ENSP00000367575.2:p.Val418=
ENST00000403558.1:c.1537_1538delinsGT	ENSP00000384420.1:p.Val513=
ENST00000528996.1:c.609_610delinsGT	ENSP00000431226.1:n.609_610delinsGT
ENST00000530113.1:n.865_866delinsGT
ENST00000531133.5:c.909_910delinsGT	ENSP00000435431.1:n.909_910delinsGT
ENST00000531797.5:c.*433_*434delinsGT	ENSP00000432554.1:n.*433_*434delinsGT
ENST00000619430.1:c.539_540delinsGT	ENSP00000478572.1:n.539_540delinsGT
NM_000062.2:c.1408_1409delinsGT , LRG_105t1:c.1408_1409delinsGT	NP_000053.2:p.Val470=
NM_001032295.1:c.1408_1409delinsGT	NP_001027466.1:p.Val470=
NM_000062.3:c.1408_1409delinsGT MANE Select	NP_000053.2:p.Val470=
NM_001032295.2:c.1408_1409delinsGT	NP_001027466.1:p.Val470=