Canonical Allele Identifier: CA223024512

Gene: SERPING1

Linked Data

• dbSNP Id: rs904412322
• gnomAD v3: 11-57614608-C-G
• gnomAD v4: 11-57614608-C-G
• MyVariant Identifiers: chr11:g.57382081C>G (hg19) ; chr11:g.57614608C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614608C>G , CM000673.2:g.57614608C>G	GRCh38
NC_000011.9:g.57382081C>G , CM000673.1:g.57382081C>G	GRCh37
NC_000011.8:g.57138657C>G	NCBI36
NG_009625.1:g.22055C>G , LRG_105:g.22055C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*27C>G MANE Select	ENSP00000278407.4:n.*27C>G
ENST00000528996.2:c.*427C>G	ENSP00000431226.2:n.*427C>G
ENST00000531605.2:c.*1306C>G	ENSP00000503752.1:n.*1306C>G
ENST00000619430.2:c.*27C>G	ENSP00000478572.2:n.*27C>G
ENST00000676670.1:c.*15+12C>G	ENSP00000504807.1:n.*15+12C>G
ENST00000676741.1:n.2612C>G
ENST00000677624.1:c.*950C>G	ENSP00000503979.1:n.*950C>G
ENST00000677625.1:c.*27C>G	ENSP00000502857.1:n.*27C>G
ENST00000677856.1:n.1783C>G
ENST00000677915.1:c.*427C>G	ENSP00000503118.1:n.*427C>G
ENST00000678533.1:c.*1072+12C>G	ENSP00000503873.1:n.*1072+12C>G
ENST00000678592.1:c.*470C>G	ENSP00000504424.1:n.*470C>G
ENST00000278407.8:c.*27C>G	ENSP00000278407.4:n.*27C>G
ENST00000340687.10:c.*27C>G	ENSP00000341861.6:n.*27C>G
ENST00000378323.8:c.*27C>G	ENSP00000367574.4:n.*27C>G
ENST00000378324.6:c.*27C>G	ENSP00000367575.2:n.*27C>G
ENST00000403558.1:c.*27C>G	ENSP00000384420.1:n.*27C>G
ENST00000528996.1:c.731C>G	ENSP00000431226.1:n.731C>G
ENST00000531797.5:c.*555C>G	ENSP00000432554.1:n.*555C>G
NM_000062.2:c.*27C>G , LRG_105t1:c.*27C>G	NP_000053.2:n.*27C>G
NM_001032295.1:c.*27C>G	NP_001027466.1:n.*27C>G
NM_000062.3:c.*27C>G MANE Select	NP_000053.2:n.*27C>G
NM_001032295.2:c.*27C>G	NP_001027466.1:n.*27C>G