Canonical Allele Identifier: CA380690907

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382020T>A (hg19) ; chr11:g.57614547T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614547T>A , CM000673.2:g.57614547T>A	GRCh38
NC_000011.9:g.57382020T>A , CM000673.1:g.57382020T>A	GRCh37
NC_000011.8:g.57138596T>A	NCBI36
NG_009625.1:g.21994T>A , LRG_105:g.21994T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1469T>A MANE Select	ENSP00000278407.4:p.Val490Asp
ENST00000528996.2:c.*366T>A	ENSP00000431226.2:n.*366T>A
ENST00000531605.2:c.*1245T>A	ENSP00000503752.1:n.*1245T>A
ENST00000619430.2:c.1265T>A	ENSP00000478572.2:p.Val422Asp
ENST00000676670.1:c.1469T>A	ENSP00000504807.1:p.Val490Asp
ENST00000676741.1:n.2551T>A
ENST00000677624.1:c.*889T>A	ENSP00000503979.1:n.*889T>A
ENST00000677625.1:c.1415T>A	ENSP00000502857.1:p.Val472Asp
ENST00000677856.1:n.1722T>A
ENST00000677915.1:c.*366T>A	ENSP00000503118.1:n.*366T>A
ENST00000678533.1:c.*1023T>A	ENSP00000503873.1:n.*1023T>A
ENST00000678592.1:c.*409T>A	ENSP00000504424.1:n.*409T>A
ENST00000278407.8:c.1469T>A	ENSP00000278407.4:p.Val490Asp
ENST00000340687.10:c.1358T>A	ENSP00000341861.6:p.Val453Asp
ENST00000378323.8:c.1484T>A	ENSP00000367574.4:p.Val495Asp
ENST00000378324.6:c.1313T>A	ENSP00000367575.2:p.Val438Asp
ENST00000403558.1:c.1598T>A	ENSP00000384420.1:p.Val533Asp
ENST00000528996.1:c.670T>A	ENSP00000431226.1:n.670T>A
ENST00000531133.5:c.970T>A	ENSP00000435431.1:n.970T>A
ENST00000531797.5:c.*494T>A	ENSP00000432554.1:n.*494T>A
ENST00000619430.1:c.600T>A	ENSP00000478572.1:n.600T>A
NM_000062.2:c.1469T>A , LRG_105t1:c.1469T>A	NP_000053.2:p.Val490Asp
NM_001032295.1:c.1469T>A	NP_001027466.1:p.Val490Asp
NM_000062.3:c.1469T>A MANE Select	NP_000053.2:p.Val490Asp
NM_001032295.2:c.1469T>A	NP_001027466.1:p.Val490Asp