Canonical Allele Identifier: CA380702505

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379231C>G (hg19) ; chr11:g.57611758C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611758C>G , CM000673.2:g.57611758C>G	GRCh38
NC_000011.9:g.57379231C>G , CM000673.1:g.57379231C>G	GRCh37
NC_000011.8:g.57135807C>G	NCBI36
NG_009625.1:g.19205C>G , LRG_105:g.19205C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1071C>G MANE Select	ENSP00000278407.4:p.Ile357Met
ENST00000528996.2:c.91C>G	ENSP00000431226.2:p.Pro31Ala
ENST00000531605.2:c.*847C>G	ENSP00000503752.1:n.*847C>G
ENST00000619430.2:c.867C>G	ENSP00000478572.2:p.Ile289Met
ENST00000676670.1:c.1071C>G	ENSP00000504807.1:p.Ile357Met
ENST00000676741.1:n.2153C>G
ENST00000677624.1:c.*491C>G	ENSP00000503979.1:n.*491C>G
ENST00000677625.1:c.1030-13C>G	ENSP00000502857.1:n.1030-13C>G
ENST00000677856.1:n.1324C>G
ENST00000677915.1:c.727C>G	ENSP00000503118.1:p.Pro243Ala
ENST00000678533.1:c.*625C>G	ENSP00000503873.1:n.*625C>G
ENST00000678592.1:c.*11C>G	ENSP00000504424.1:n.*11C>G
ENST00000278407.8:c.1071C>G	ENSP00000278407.4:p.Ile357Met
ENST00000340687.10:c.1030-70C>G	ENSP00000341861.6:n.1030-70C>G
ENST00000378323.8:c.1086C>G	ENSP00000367574.4:p.Ile362Met
ENST00000378324.6:c.915C>G	ENSP00000367575.2:p.Ile305Met
ENST00000403558.1:c.1200C>G	ENSP00000384420.1:p.Ile400Met
ENST00000528996.1:c.272C>G	ENSP00000431226.1:n.272C>G
ENST00000530113.1:n.528C>G
ENST00000531133.5:c.572C>G	ENSP00000435431.1:n.572C>G
ENST00000531797.5:c.*96C>G	ENSP00000432554.1:n.*96C>G
ENST00000619430.1:c.349-147C>G	ENSP00000478572.1:n.349-147C>G
NM_000062.2:c.1071C>G , LRG_105t1:c.1071C>G	NP_000053.2:p.Ile357Met
NM_001032295.1:c.1071C>G	NP_001027466.1:p.Ile357Met
NM_000062.3:c.1071C>G MANE Select	NP_000053.2:p.Ile357Met
NM_001032295.2:c.1071C>G	NP_001027466.1:p.Ile357Met