Canonical Allele Identifier: CA380690941

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382037T>G (hg19) ; chr11:g.57614564T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614564T>G , CM000673.2:g.57614564T>G	GRCh38
NC_000011.9:g.57382037T>G , CM000673.1:g.57382037T>G	GRCh37
NC_000011.8:g.57138613T>G	NCBI36
NG_009625.1:g.22011T>G , LRG_105:g.22011T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1486T>G MANE Select	ENSP00000278407.4:p.Tyr496Asp
ENST00000528996.2:c.*383T>G	ENSP00000431226.2:n.*383T>G
ENST00000531605.2:c.*1262T>G	ENSP00000503752.1:n.*1262T>G
ENST00000619430.2:c.1282T>G	ENSP00000478572.2:p.Tyr428Asp
ENST00000676670.1:c.1486T>G	ENSP00000504807.1:p.Tyr496Asp
ENST00000676741.1:n.2568T>G
ENST00000677624.1:c.*906T>G	ENSP00000503979.1:n.*906T>G
ENST00000677625.1:c.1432T>G	ENSP00000502857.1:p.Tyr478Asp
ENST00000677856.1:n.1739T>G
ENST00000677915.1:c.*383T>G	ENSP00000503118.1:n.*383T>G
ENST00000678533.1:c.*1040T>G	ENSP00000503873.1:n.*1040T>G
ENST00000678592.1:c.*426T>G	ENSP00000504424.1:n.*426T>G
ENST00000278407.8:c.1486T>G	ENSP00000278407.4:p.Tyr496Asp
ENST00000340687.10:c.1375T>G	ENSP00000341861.6:p.Tyr459Asp
ENST00000378323.8:c.1501T>G	ENSP00000367574.4:p.Tyr501Asp
ENST00000378324.6:c.1330T>G	ENSP00000367575.2:p.Tyr444Asp
ENST00000403558.1:c.1615T>G	ENSP00000384420.1:p.Tyr539Asp
ENST00000528996.1:c.687T>G	ENSP00000431226.1:n.687T>G
ENST00000531133.5:c.987T>G	ENSP00000435431.1:n.987T>G
ENST00000531797.5:c.*511T>G	ENSP00000432554.1:n.*511T>G
ENST00000619430.1:c.617T>G	ENSP00000478572.1:n.617T>G
NM_000062.2:c.1486T>G , LRG_105t1:c.1486T>G	NP_000053.2:p.Tyr496Asp
NM_001032295.1:c.1486T>G	NP_001027466.1:p.Tyr496Asp
NM_000062.3:c.1486T>G MANE Select	NP_000053.2:p.Tyr496Asp
NM_001032295.2:c.1486T>G	NP_001027466.1:p.Tyr496Asp