Canonical Allele Identifier: CA1975536843

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611722_57611737delinsGCAGCTGCAGCTCTCC , CM000673.2:g.57611722_57611737delinsGCAGCTGCAGCTCTCC	GRCh38
NC_000011.9:g.57379195_57379210delinsGCAGCTGCAGCTCTCC , CM000673.1:g.57379195_57379210delinsGCAGCTGCAGCTCTCC	GRCh37
NC_000011.8:g.57135771_57135786delinsGCAGCTGCAGCTCTCC	NCBI36
NG_009625.1:g.19169_19184delinsGCAGCTGCAGCTCTCC , LRG_105:g.19169_19184delinsGCAGCTGCAGCTCTCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1035_1050delinsGCAGCTGCAGCTCTCC MANE Select	ENSP00000278407.4:p.Gly345=
ENST00000528996.2:c.59-4_70delinsGCAGCTGCAGCTCTCC
ENST00000531605.2:c.*811_*826delinsGCAGCTGCAGCTCTCC	ENSP00000503752.1:n.*811_*826delinsGCAGCTGCAGCTCTCC
ENST00000619430.2:c.831_846delinsGCAGCTGCAGCTCTCC	ENSP00000478572.2:p.Gly277=
ENST00000676670.1:c.1035_1050delinsGCAGCTGCAGCTCTCC	ENSP00000504807.1:p.Gly345=
ENST00000676741.1:n.2117_2132delinsGCAGCTGCAGCTCTCC
ENST00000677624.1:c.*455_*470delinsGCAGCTGCAGCTCTCC	ENSP00000503979.1:n.*455_*470delinsGCAGCTGCAGCTCTCC
ENST00000677625.1:c.1030-49_1030-34delinsGCAGCTGCAGCTCTCC	ENSP00000502857.1:n.1030-49_1030-34delinsGCAGCTGCAGCTCTCC
ENST00000677856.1:n.1288_1303delinsGCAGCTGCAGCTCTCC
ENST00000677915.1:c.691_706delinsGCAGCTGCAGCTCTCC	ENSP00000503118.1:p.Ala231=
ENST00000678533.1:c.*589_*604delinsGCAGCTGCAGCTCTCC	ENSP00000503873.1:n.*589_*604delinsGCAGCTGCAGCTCTCC
ENST00000678592.1:c.1124_1139delinsGCAGCTGCAGCTCTCC	ENSP00000504424.1:p.Gly375=
ENST00000278407.8:c.1035_1050delinsGCAGCTGCAGCTCTCC	ENSP00000278407.4:p.Gly345=
ENST00000340687.10:c.1030-106_1030-91delinsGCAGCTGCAGCTCTCC	ENSP00000341861.6:n.1030-106_1030-91delinsGCAGCTGCAGCTCTCC
ENST00000378323.8:c.1050_1065delinsGCAGCTGCAGCTCTCC	ENSP00000367574.4:p.Gly350=
ENST00000378324.6:c.879_894delinsGCAGCTGCAGCTCTCC	ENSP00000367575.2:p.Gly293=
ENST00000403558.1:c.1164_1179delinsGCAGCTGCAGCTCTCC	ENSP00000384420.1:p.Gly388=
ENST00000528996.1:c.236_251delinsGCAGCTGCAGCTCTCC	ENSP00000431226.1:p.Gly79=
ENST00000530113.1:n.492_507delinsGCAGCTGCAGCTCTCC
ENST00000531133.5:c.536_551delinsGCAGCTGCAGCTCTCC	ENSP00000435431.1:n.536_551delinsGCAGCTGCAGCTCTCC
ENST00000531797.5:c.*60_*75delinsGCAGCTGCAGCTCTCC	ENSP00000432554.1:n.*60_*75delinsGCAGCTGCAGCTCTCC
ENST00000619430.1:c.349-183_349-168delinsGCAGCTGCAGCTCTCC	ENSP00000478572.1:n.349-183_349-168delinsGCAGCTGCAGCTCTCC
NM_000062.2:c.1035_1050delinsGCAGCTGCAGCTCTCC , LRG_105t1:c.1035_1050delinsGCAGCTGCAGCTCTCC	NP_000053.2:p.Gly345=
NM_001032295.1:c.1035_1050delinsGCAGCTGCAGCTCTCC	NP_001027466.1:p.Gly345=
NM_000062.3:c.1035_1050delinsGCAGCTGCAGCTCTCC MANE Select	NP_000053.2:p.Gly345=
NM_001032295.2:c.1035_1050delinsGCAGCTGCAGCTCTCC	NP_001027466.1:p.Gly345=