Canonical Allele Identifier: CA6008039

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 3006949
• ClinVar RCV Id: RCV003861564
• dbSNP Id: rs541933653
• ExAC: 11:57367759 C / G
• gnomAD v2: 11-57367759-C-G
• gnomAD v3: 11-57600286-C-G
• gnomAD v4: 11-57600286-C-G
• MyVariant Identifiers: chr11:g.57367759C>G (hg19) ; chr11:g.57600286C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600286C>G , CM000673.2:g.57600286C>G	GRCh38
NC_000011.9:g.57367759C>G , CM000673.1:g.57367759C>G	GRCh37
NC_000011.8:g.57124335C>G	NCBI36
NG_009625.1:g.7733C>G , LRG_105:g.7733C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.459C>G MANE Select	ENSP00000278407.4:p.Leu153=
ENST00000528996.2:c.58+1958C>G	ENSP00000431226.2:n.58+1958C>G
ENST00000531605.2:c.52-1749C>G	ENSP00000503752.1:n.52-1749C>G
ENST00000619430.2:c.459C>G	ENSP00000478572.2:p.Leu153=
ENST00000676670.1:c.459C>G	ENSP00000504807.1:p.Leu153=
ENST00000676741.1:n.1541C>G
ENST00000677275.1:n.446C>G
ENST00000677624.1:c.459C>G	ENSP00000503979.1:p.Leu153=
ENST00000677625.1:c.459C>G	ENSP00000502857.1:p.Leu153=
ENST00000677856.1:n.518C>G
ENST00000677915.1:c.459C>G	ENSP00000503118.1:p.Leu153=
ENST00000678533.1:c.52-1749C>G	ENSP00000503873.1:n.52-1749C>G
ENST00000678592.1:c.459C>G	ENSP00000504424.1:p.Leu153=
ENST00000278407.8:c.459C>G	ENSP00000278407.4:p.Leu153=
ENST00000340687.10:c.459C>G	ENSP00000341861.6:p.Leu153=
ENST00000378323.8:c.474C>G	ENSP00000367574.4:p.Leu158=
ENST00000378324.6:c.303C>G	ENSP00000367575.2:p.Leu101=
ENST00000403558.1:c.561C>G	ENSP00000384420.1:p.Leu187=
ENST00000405496.5:c.459C>G	ENSP00000384561.1:p.Leu153=
ENST00000531133.5:c.52-1749C>G	ENSP00000435431.1:n.52-1749C>G
ENST00000531797.5:c.52-1749C>G	ENSP00000432554.1:n.52-1749C>G
ENST00000619430.1:c.348+111C>G	ENSP00000478572.1:n.348+111C>G
NM_000062.2:c.459C>G , LRG_105t1:c.459C>G	NP_000053.2:p.Leu153=
NM_001032295.1:c.459C>G	NP_001027466.1:p.Leu153=
NM_000062.3:c.459C>G MANE Select	NP_000053.2:p.Leu153=
NM_001032295.2:c.459C>G	NP_001027466.1:p.Leu153=