Canonical Allele Identifier: CA2541480591

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614587del , CM000673.2:g.57614587del	GRCh38
NC_000011.9:g.57382060del , CM000673.1:g.57382060del	GRCh37
NC_000011.8:g.57138636del	NCBI36
NG_009625.1:g.22034del , LRG_105:g.22034del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*6del MANE Select	ENSP00000278407.4:n.*6del
ENST00000528996.2:c.*406del	ENSP00000431226.2:n.*406del
ENST00000531605.2:c.*1285del	ENSP00000503752.1:n.*1285del
ENST00000619430.2:c.*6del	ENSP00000478572.2:n.*6del
ENST00000676670.1:c.*6del	ENSP00000504807.1:n.*6del
ENST00000676741.1:n.2591del
ENST00000677624.1:c.*929del	ENSP00000503979.1:n.*929del
ENST00000677625.1:c.*6del	ENSP00000502857.1:n.*6del
ENST00000677856.1:n.1762del
ENST00000677915.1:c.*406del	ENSP00000503118.1:n.*406del
ENST00000678533.1:c.*1063del	ENSP00000503873.1:n.*1063del
ENST00000678592.1:c.*449del	ENSP00000504424.1:n.*449del
ENST00000278407.8:c.*6del	ENSP00000278407.4:n.*6del
ENST00000340687.10:c.*6del	ENSP00000341861.6:n.*6del
ENST00000378323.8:c.*6del	ENSP00000367574.4:n.*6del
ENST00000378324.6:c.*6del	ENSP00000367575.2:n.*6del
ENST00000403558.1:c.*6del	ENSP00000384420.1:n.*6del
ENST00000528996.1:c.710del	ENSP00000431226.1:n.710del
ENST00000531797.5:c.*534del	ENSP00000432554.1:n.*534del
NM_000062.2:c.*6del , LRG_105t1:c.*6del	NP_000053.2:n.*6del
NM_001032295.1:c.*6del	NP_001027466.1:n.*6del
NM_000062.3:c.*6del MANE Select	NP_000053.2:n.*6del
NM_001032295.2:c.*6del	NP_001027466.1:n.*6del