Canonical Allele Identifier: CA2832528697

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600350_57600353delinsTG , CM000673.2:g.57600350_57600353delinsTG	GRCh38
NC_000011.9:g.57367823_57367826delinsTG , CM000673.1:g.57367823_57367826delinsTG	GRCh37
NC_000011.8:g.57124399_57124402delinsTG	NCBI36
NG_009625.1:g.7797_7800delinsTG , LRG_105:g.7797_7800delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.523_526delinsTG MANE Select	ENSP00000278407.4:p.Ala175TrpfsTer?
ENST00000528996.2:c.58+2022_58+2025delinsTG	ENSP00000431226.2:n.58+2022_58+2025delinsTG
ENST00000531605.2:c.52-1685_52-1682delinsTG	ENSP00000503752.1:n.52-1685_52-1682delinsTG
ENST00000619430.2:c.523_526delinsTG	ENSP00000478572.2:p.Ala175TrpfsTer?
ENST00000676670.1:c.523_526delinsTG	ENSP00000504807.1:p.Ala175TrpfsTer?
ENST00000676741.1:n.1605_1608delinsTG
ENST00000677275.1:n.510_513delinsTG
ENST00000677624.1:c.523_526delinsTG	ENSP00000503979.1:p.Ala175TrpfsTer?
ENST00000677625.1:c.523_526delinsTG	ENSP00000502857.1:p.Ala175TrpfsTer?
ENST00000677856.1:n.582_585delinsTG
ENST00000677915.1:c.523_526delinsTG	ENSP00000503118.1:p.Ala175TrpfsTer?
ENST00000678533.1:c.52-1685_52-1682delinsTG	ENSP00000503873.1:n.52-1685_52-1682delinsTG
ENST00000678592.1:c.523_526delinsTG	ENSP00000504424.1:p.Ala175TrpfsTer?
ENST00000278407.8:c.523_526delinsTG	ENSP00000278407.4:p.Ala175TrpfsTer?
ENST00000340687.10:c.523_526delinsTG	ENSP00000341861.6:p.Ala175TrpfsTer?
ENST00000378323.8:c.538_541delinsTG	ENSP00000367574.4:p.Ala180TrpfsTer?
ENST00000378324.6:c.367_370delinsTG	ENSP00000367575.2:p.Ala123TrpfsTer?
ENST00000403558.1:c.625_628delinsTG	ENSP00000384420.1:p.Ala209TrpfsTer?
ENST00000531133.5:c.52-1685_52-1682delinsTG	ENSP00000435431.1:n.52-1685_52-1682delinsTG
ENST00000531797.5:c.52-1685_52-1682delinsTG	ENSP00000432554.1:n.52-1685_52-1682delinsTG
ENST00000619430.1:c.348+175_348+178delinsTG	ENSP00000478572.1:n.348+175_348+178delinsTG
NM_000062.2:c.523_526delinsTG , LRG_105t1:c.523_526delinsTG	NP_000053.2:p.Ala175TrpfsTer?
NM_001032295.1:c.523_526delinsTG	NP_001027466.1:p.Ala175TrpfsTer?
NM_000062.3:c.523_526delinsTG MANE Select	NP_000053.2:p.Ala175TrpfsTer?
NM_001032295.2:c.523_526delinsTG	NP_001027466.1:p.Ala175TrpfsTer?