Canonical Allele Identifier: CA2613603664

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614661-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614661A>G , CM000673.2:g.57614661A>G	GRCh38
NC_000011.9:g.57382134A>G , CM000673.1:g.57382134A>G	GRCh37
NC_000011.8:g.57138710A>G	NCBI36
NG_009625.1:g.22108A>G , LRG_105:g.22108A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*80A>G MANE Select	ENSP00000278407.4:n.*80A>G
ENST00000528996.2:c.*480A>G	ENSP00000431226.2:n.*480A>G
ENST00000531605.2:c.*1359A>G	ENSP00000503752.1:n.*1359A>G
ENST00000619430.2:c.*80A>G	ENSP00000478572.2:n.*80A>G
ENST00000676670.1:c.*15+65A>G	ENSP00000504807.1:n.*15+65A>G
ENST00000676741.1:n.2665A>G
ENST00000677624.1:c.*1003A>G	ENSP00000503979.1:n.*1003A>G
ENST00000677625.1:c.*80A>G	ENSP00000502857.1:n.*80A>G
ENST00000677856.1:n.1836A>G
ENST00000677915.1:c.*480A>G	ENSP00000503118.1:n.*480A>G
ENST00000678533.1:c.*1072+65A>G	ENSP00000503873.1:n.*1072+65A>G
ENST00000678592.1:c.*523A>G	ENSP00000504424.1:n.*523A>G
ENST00000278407.8:c.*80A>G	ENSP00000278407.4:n.*80A>G
ENST00000340687.10:c.*80A>G	ENSP00000341861.6:n.*80A>G
ENST00000378323.8:c.*80A>G	ENSP00000367574.4:n.*80A>G
ENST00000378324.6:c.*80A>G	ENSP00000367575.2:n.*80A>G
ENST00000403558.1:c.*80A>G	ENSP00000384420.1:n.*80A>G
ENST00000528996.1:c.784A>G	ENSP00000431226.1:n.784A>G
ENST00000531797.5:c.*608A>G	ENSP00000432554.1:n.*608A>G
NM_000062.2:c.*80A>G , LRG_105t1:c.*80A>G	NP_000053.2:n.*80A>G
NM_001032295.1:c.*80A>G	NP_001027466.1:n.*80A>G
NM_000062.3:c.*80A>G MANE Select	NP_000053.2:n.*80A>G
NM_001032295.2:c.*80A>G	NP_001027466.1:n.*80A>G