Canonical Allele Identifier: CA678581271

Gene: SERPING1

Linked Data

• dbSNP Id: rs1165804047
• gnomAD v3: 11-57614749-G-A
• gnomAD v4: 11-57614749-G-A
• MyVariant Identifiers: chr11:g.57382222G>A (hg19) ; chr11:g.57614749G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614749G>A , CM000673.2:g.57614749G>A	GRCh38
NC_000011.9:g.57382222G>A , CM000673.1:g.57382222G>A	GRCh37
NC_000011.8:g.57138798G>A	NCBI36
NG_009625.1:g.22196G>A , LRG_105:g.22196G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*168G>A MANE Select	ENSP00000278407.4:n.*168G>A
ENST00000528996.2:c.*568G>A	ENSP00000431226.2:n.*568G>A
ENST00000531605.2:c.*1447G>A	ENSP00000503752.1:n.*1447G>A
ENST00000619430.2:c.*168G>A	ENSP00000478572.2:n.*168G>A
ENST00000676670.1:c.*15+153G>A	ENSP00000504807.1:n.*15+153G>A
ENST00000676741.1:n.2753G>A
ENST00000677624.1:c.*1091G>A	ENSP00000503979.1:n.*1091G>A
ENST00000677625.1:c.*168G>A	ENSP00000502857.1:n.*168G>A
ENST00000677856.1:n.1924G>A
ENST00000677915.1:c.*568G>A	ENSP00000503118.1:n.*568G>A
ENST00000678533.1:c.*1072+153G>A	ENSP00000503873.1:n.*1072+153G>A
ENST00000678592.1:c.*611G>A	ENSP00000504424.1:n.*611G>A
ENST00000278407.8:c.*168G>A	ENSP00000278407.4:n.*168G>A
ENST00000340687.10:c.*168G>A	ENSP00000341861.6:n.*168G>A
ENST00000378324.6:c.*168G>A	ENSP00000367575.2:n.*168G>A
ENST00000403558.1:c.*168G>A	ENSP00000384420.1:n.*168G>A
ENST00000528996.1:c.872G>A	ENSP00000431226.1:n.872G>A
ENST00000531797.5:c.*696G>A	ENSP00000432554.1:n.*696G>A
NM_000062.2:c.*168G>A , LRG_105t1:c.*168G>A	NP_000053.2:n.*168G>A
NM_001032295.1:c.*168G>A	NP_001027466.1:n.*168G>A
NM_000062.3:c.*168G>A MANE Select	NP_000053.2:n.*168G>A
NM_001032295.2:c.*168G>A	NP_001027466.1:n.*168G>A