Canonical Allele Identifier: CA2695214283

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614552del , CM000673.2:g.57614552del	GRCh38
NC_000011.9:g.57382025del , CM000673.1:g.57382025del	GRCh37
NC_000011.8:g.57138601del	NCBI36
NG_009625.1:g.21999del , LRG_105:g.21999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1474del MANE Select	ENSP00000278407.4:p.Met492TrpfsTer?
ENST00000528996.2:c.*371del	ENSP00000431226.2:n.*371del
ENST00000531605.2:c.*1250del	ENSP00000503752.1:n.*1250del
ENST00000619430.2:c.1270del	ENSP00000478572.2:p.Met424TrpfsTer?
ENST00000676670.1:c.1474del	ENSP00000504807.1:p.Met492TrpfsTer?
ENST00000676741.1:n.2556del
ENST00000677624.1:c.*894del	ENSP00000503979.1:n.*894del
ENST00000677625.1:c.1420del	ENSP00000502857.1:p.Met474TrpfsTer?
ENST00000677856.1:n.1727del
ENST00000677915.1:c.*371del	ENSP00000503118.1:n.*371del
ENST00000678533.1:c.*1028del	ENSP00000503873.1:n.*1028del
ENST00000678592.1:c.*414del	ENSP00000504424.1:n.*414del
ENST00000278407.8:c.1474del	ENSP00000278407.4:p.Met492TrpfsTer?
ENST00000340687.10:c.1363del	ENSP00000341861.6:p.Met455TrpfsTer?
ENST00000378323.8:c.1489del	ENSP00000367574.4:p.Met497TrpfsTer?
ENST00000378324.6:c.1318del	ENSP00000367575.2:p.Met440TrpfsTer?
ENST00000403558.1:c.1603del	ENSP00000384420.1:p.Met535TrpfsTer?
ENST00000528996.1:c.675del	ENSP00000431226.1:n.675del
ENST00000531133.5:c.975del	ENSP00000435431.1:n.975del
ENST00000531797.5:c.*499del	ENSP00000432554.1:n.*499del
ENST00000619430.1:c.605del	ENSP00000478572.1:n.605del
NM_000062.2:c.1474del , LRG_105t1:c.1474del	NP_000053.2:p.Met492TrpfsTer?
NM_001032295.1:c.1474del	NP_001027466.1:p.Met492TrpfsTer?
NM_000062.3:c.1474del MANE Select	NP_000053.2:p.Met492TrpfsTer?
NM_001032295.2:c.1474del	NP_001027466.1:p.Met492TrpfsTer?