Canonical Allele Identifier: CA380699694

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373660T>A (hg19) ; chr11:g.57606187T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606187T>A , CM000673.2:g.57606187T>A	GRCh38
NC_000011.9:g.57373660T>A , CM000673.1:g.57373660T>A	GRCh37
NC_000011.8:g.57130236T>A	NCBI36
NG_009625.1:g.13634T>A , LRG_105:g.13634T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.863T>A MANE Select	ENSP00000278407.4:p.Val288Asp
ENST00000528996.2:c.59-5539T>A	ENSP00000431226.2:n.59-5539T>A
ENST00000531605.2:c.*639T>A	ENSP00000503752.1:n.*639T>A
ENST00000619430.2:c.686-221T>A	ENSP00000478572.2:n.686-221T>A
ENST00000676670.1:c.863T>A	ENSP00000504807.1:p.Val288Asp
ENST00000676741.1:n.1945T>A
ENST00000677624.1:c.*283T>A	ENSP00000503979.1:n.*283T>A
ENST00000677625.1:c.863T>A	ENSP00000502857.1:p.Val288Asp
ENST00000677856.1:n.922T>A
ENST00000677915.1:c.685+4018T>A	ENSP00000503118.1:n.685+4018T>A
ENST00000678533.1:c.*417T>A	ENSP00000503873.1:n.*417T>A
ENST00000678592.1:c.863T>A	ENSP00000504424.1:p.Val288Asp
ENST00000278407.8:c.863T>A	ENSP00000278407.4:p.Val288Asp
ENST00000340687.10:c.863T>A	ENSP00000341861.6:p.Val288Asp
ENST00000378323.8:c.878T>A	ENSP00000367574.4:p.Val293Asp
ENST00000378324.6:c.707T>A	ENSP00000367575.2:p.Val236Asp
ENST00000403558.1:c.965T>A	ENSP00000384420.1:p.Val322Asp
ENST00000531133.5:c.364T>A	ENSP00000435431.1:n.364T>A
ENST00000531797.5:c.*54+4018T>A	ENSP00000432554.1:n.*54+4018T>A
ENST00000619430.1:c.349-5718T>A	ENSP00000478572.1:n.349-5718T>A
NM_000062.2:c.863T>A , LRG_105t1:c.863T>A	NP_000053.2:p.Val288Asp
NM_001032295.1:c.863T>A	NP_001027466.1:p.Val288Asp
NM_000062.3:c.863T>A MANE Select	NP_000053.2:p.Val288Asp
NM_001032295.2:c.863T>A	NP_001027466.1:p.Val288Asp