Canonical Allele Identifier: CA380690957

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382044C>G (hg19) ; chr11:g.57614571C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614571C>G , CM000673.2:g.57614571C>G	GRCh38
NC_000011.9:g.57382044C>G , CM000673.1:g.57382044C>G	GRCh37
NC_000011.8:g.57138620C>G	NCBI36
NG_009625.1:g.22018C>G , LRG_105:g.22018C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1493C>G MANE Select	ENSP00000278407.4:p.Pro498Arg
ENST00000528996.2:c.*390C>G	ENSP00000431226.2:n.*390C>G
ENST00000531605.2:c.*1269C>G	ENSP00000503752.1:n.*1269C>G
ENST00000619430.2:c.1289C>G	ENSP00000478572.2:p.Pro430Arg
ENST00000676670.1:c.1493C>G	ENSP00000504807.1:p.Pro498Arg
ENST00000676741.1:n.2575C>G
ENST00000677624.1:c.*913C>G	ENSP00000503979.1:n.*913C>G
ENST00000677625.1:c.1439C>G	ENSP00000502857.1:p.Pro480Arg
ENST00000677856.1:n.1746C>G
ENST00000677915.1:c.*390C>G	ENSP00000503118.1:n.*390C>G
ENST00000678533.1:c.*1047C>G	ENSP00000503873.1:n.*1047C>G
ENST00000678592.1:c.*433C>G	ENSP00000504424.1:n.*433C>G
ENST00000278407.8:c.1493C>G	ENSP00000278407.4:p.Pro498Arg
ENST00000340687.10:c.1382C>G	ENSP00000341861.6:p.Pro461Arg
ENST00000378323.8:c.1508C>G	ENSP00000367574.4:p.Pro503Arg
ENST00000378324.6:c.1337C>G	ENSP00000367575.2:p.Pro446Arg
ENST00000403558.1:c.1622C>G	ENSP00000384420.1:p.Pro541Arg
ENST00000528996.1:c.694C>G	ENSP00000431226.1:n.694C>G
ENST00000531133.5:c.994C>G	ENSP00000435431.1:n.994C>G
ENST00000531797.5:c.*518C>G	ENSP00000432554.1:n.*518C>G
ENST00000619430.1:c.624C>G	ENSP00000478572.1:n.624C>G
NM_000062.2:c.1493C>G , LRG_105t1:c.1493C>G	NP_000053.2:p.Pro498Arg
NM_001032295.1:c.1493C>G	NP_001027466.1:p.Pro498Arg
NM_000062.3:c.1493C>G MANE Select	NP_000053.2:p.Pro498Arg
NM_001032295.2:c.1493C>G	NP_001027466.1:p.Pro498Arg