Canonical Allele Identifier: CA380690736

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381944G>C (hg19) ; chr11:g.57614471G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614471G>C , CM000673.2:g.57614471G>C	GRCh38
NC_000011.9:g.57381944G>C , CM000673.1:g.57381944G>C	GRCh37
NC_000011.8:g.57138520G>C	NCBI36
NG_009625.1:g.21918G>C , LRG_105:g.21918G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1393G>C MANE Select	ENSP00000278407.4:p.Ala465Pro
ENST00000528996.2:c.*290G>C	ENSP00000431226.2:n.*290G>C
ENST00000531605.2:c.*1169G>C	ENSP00000503752.1:n.*1169G>C
ENST00000619430.2:c.1189G>C	ENSP00000478572.2:p.Ala397Pro
ENST00000676670.1:c.1393G>C	ENSP00000504807.1:p.Ala465Pro
ENST00000676741.1:n.2475G>C
ENST00000677624.1:c.*813G>C	ENSP00000503979.1:n.*813G>C
ENST00000677625.1:c.1339G>C	ENSP00000502857.1:p.Ala447Pro
ENST00000677856.1:n.1646G>C
ENST00000677915.1:c.*290G>C	ENSP00000503118.1:n.*290G>C
ENST00000678533.1:c.*947G>C	ENSP00000503873.1:n.*947G>C
ENST00000678592.1:c.*333G>C	ENSP00000504424.1:n.*333G>C
ENST00000278407.8:c.1393G>C	ENSP00000278407.4:p.Ala465Pro
ENST00000340687.10:c.1282G>C	ENSP00000341861.6:p.Ala428Pro
ENST00000378323.8:c.1408G>C	ENSP00000367574.4:p.Ala470Pro
ENST00000378324.6:c.1237G>C	ENSP00000367575.2:p.Ala413Pro
ENST00000403558.1:c.1522G>C	ENSP00000384420.1:p.Ala508Pro
ENST00000528996.1:c.594G>C	ENSP00000431226.1:n.594G>C
ENST00000530113.1:n.850G>C
ENST00000531133.5:c.894G>C	ENSP00000435431.1:n.894G>C
ENST00000531797.5:c.*418G>C	ENSP00000432554.1:n.*418G>C
ENST00000619430.1:c.524G>C	ENSP00000478572.1:n.524G>C
NM_000062.2:c.1393G>C , LRG_105t1:c.1393G>C	NP_000053.2:p.Ala465Pro
NM_001032295.1:c.1393G>C	NP_001027466.1:p.Ala465Pro
NM_000062.3:c.1393G>C MANE Select	NP_000053.2:p.Ala465Pro
NM_001032295.2:c.1393G>C	NP_001027466.1:p.Ala465Pro