Canonical Allele Identifier: CA380695365

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57367739G>A (hg19) ; chr11:g.57600266G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600266G>A , CM000673.2:g.57600266G>A	GRCh38
NC_000011.9:g.57367739G>A , CM000673.1:g.57367739G>A	GRCh37
NC_000011.8:g.57124315G>A	NCBI36
NG_009625.1:g.7713G>A , LRG_105:g.7713G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.439G>A MANE Select	ENSP00000278407.4:p.Val147Ile
ENST00000528996.2:c.58+1938G>A	ENSP00000431226.2:n.58+1938G>A
ENST00000531605.2:c.52-1769G>A	ENSP00000503752.1:n.52-1769G>A
ENST00000619430.2:c.439G>A	ENSP00000478572.2:p.Val147Ile
ENST00000676670.1:c.439G>A	ENSP00000504807.1:p.Val147Ile
ENST00000676741.1:n.1521G>A
ENST00000677275.1:n.426G>A
ENST00000677624.1:c.439G>A	ENSP00000503979.1:p.Val147Ile
ENST00000677625.1:c.439G>A	ENSP00000502857.1:p.Val147Ile
ENST00000677856.1:n.498G>A
ENST00000677915.1:c.439G>A	ENSP00000503118.1:p.Val147Ile
ENST00000678533.1:c.52-1769G>A	ENSP00000503873.1:n.52-1769G>A
ENST00000678592.1:c.439G>A	ENSP00000504424.1:p.Val147Ile
ENST00000278407.8:c.439G>A	ENSP00000278407.4:p.Val147Ile
ENST00000340687.10:c.439G>A	ENSP00000341861.6:p.Val147Ile
ENST00000378323.8:c.454G>A	ENSP00000367574.4:p.Val152Ile
ENST00000378324.6:c.283G>A	ENSP00000367575.2:p.Val95Ile
ENST00000403558.1:c.541G>A	ENSP00000384420.1:p.Val181Ile
ENST00000405496.5:c.439G>A	ENSP00000384561.1:p.Val147Ile
ENST00000531133.5:c.52-1769G>A	ENSP00000435431.1:n.52-1769G>A
ENST00000531797.5:c.52-1769G>A	ENSP00000432554.1:n.52-1769G>A
ENST00000619430.1:c.348+91G>A	ENSP00000478572.1:n.348+91G>A
NM_000062.2:c.439G>A , LRG_105t1:c.439G>A	NP_000053.2:p.Val147Ile
NM_001032295.1:c.439G>A	NP_001027466.1:p.Val147Ile
NM_000062.3:c.439G>A MANE Select	NP_000053.2:p.Val147Ile
NM_001032295.2:c.439G>A	NP_001027466.1:p.Val147Ile