Canonical Allele Identifier: CA380699012

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 2900272
• ClinVar RCV Id: RCV003737069
• dbSNP Id: rs1338839404
• gnomAD v2: 11-57373558-A-G
• gnomAD v4: 11-57606085-A-G
• MyVariant Identifiers: chr11:g.57373558A>G (hg19) ; chr11:g.57606085A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606085A>G , CM000673.2:g.57606085A>G	GRCh38
NC_000011.9:g.57373558A>G , CM000673.1:g.57373558A>G	GRCh37
NC_000011.8:g.57130134A>G	NCBI36
NG_009625.1:g.13532A>G , LRG_105:g.13532A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.761A>G MANE Select	ENSP00000278407.4:p.Asn254Ser
ENST00000528996.2:c.59-5641A>G	ENSP00000431226.2:n.59-5641A>G
ENST00000531605.2:c.*537A>G	ENSP00000503752.1:n.*537A>G
ENST00000619430.2:c.686-323A>G	ENSP00000478572.2:n.686-323A>G
ENST00000676670.1:c.761A>G	ENSP00000504807.1:p.Asn254Ser
ENST00000676741.1:n.1843A>G
ENST00000677624.1:c.*181A>G	ENSP00000503979.1:n.*181A>G
ENST00000677625.1:c.761A>G	ENSP00000502857.1:p.Asn254Ser
ENST00000677856.1:n.820A>G
ENST00000677915.1:c.685+3916A>G	ENSP00000503118.1:n.685+3916A>G
ENST00000678533.1:c.*315A>G	ENSP00000503873.1:n.*315A>G
ENST00000678592.1:c.761A>G	ENSP00000504424.1:p.Asn254Ser
ENST00000278407.8:c.761A>G	ENSP00000278407.4:p.Asn254Ser
ENST00000340687.10:c.761A>G	ENSP00000341861.6:p.Asn254Ser
ENST00000378323.8:c.776A>G	ENSP00000367574.4:p.Asn259Ser
ENST00000378324.6:c.605A>G	ENSP00000367575.2:p.Asn202Ser
ENST00000403558.1:c.863A>G	ENSP00000384420.1:p.Asn288Ser
ENST00000531133.5:c.262A>G	ENSP00000435431.1:n.262A>G
ENST00000531797.5:c.*54+3916A>G	ENSP00000432554.1:n.*54+3916A>G
ENST00000619430.1:c.349-5820A>G	ENSP00000478572.1:n.349-5820A>G
NM_000062.2:c.761A>G , LRG_105t1:c.761A>G	NP_000053.2:p.Asn254Ser
NM_001032295.1:c.761A>G	NP_001027466.1:p.Asn254Ser
NM_000062.3:c.761A>G MANE Select	NP_000053.2:p.Asn254Ser
NM_001032295.2:c.761A>G	NP_001027466.1:p.Asn254Ser