Canonical Allele Identifier: CA474568317

Gene: SERPING1

Linked Data

• dbSNP Id: rs747078135
• gnomAD v4: 11-57611866-C-G
• MyVariant Identifiers: chr11:g.57379339C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611866C>G , CM000673.2:g.57611866C>G	GRCh38
NC_000011.9:g.57379339C>G , CM000673.1:g.57379339C>G	GRCh37
NC_000011.8:g.57135915C>G	NCBI36
NG_009625.1:g.19313C>G , LRG_105:g.19313C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1179C>G MANE Select	ENSP00000278407.4:p.Pro393=
ENST00000528996.2:c.*76C>G	ENSP00000431226.2:n.*76C>G
ENST00000531605.2:c.*955C>G	ENSP00000503752.1:n.*955C>G
ENST00000619430.2:c.975C>G	ENSP00000478572.2:p.Pro325=
ENST00000676670.1:c.1179C>G	ENSP00000504807.1:p.Pro393=
ENST00000676741.1:n.2261C>G
ENST00000677624.1:c.*599C>G	ENSP00000503979.1:n.*599C>G
ENST00000677625.1:c.1125C>G	ENSP00000502857.1:p.Pro375=
ENST00000677856.1:n.1432C>G
ENST00000677915.1:c.*76C>G	ENSP00000503118.1:n.*76C>G
ENST00000678533.1:c.*733C>G	ENSP00000503873.1:n.*733C>G
ENST00000678592.1:c.*119C>G	ENSP00000504424.1:n.*119C>G
ENST00000278407.8:c.1179C>G	ENSP00000278407.4:p.Pro393=
ENST00000340687.10:c.1068C>G	ENSP00000341861.6:p.Pro356=
ENST00000378323.8:c.1194C>G	ENSP00000367574.4:p.Pro398=
ENST00000378324.6:c.1023C>G	ENSP00000367575.2:p.Pro341=
ENST00000403558.1:c.1308C>G	ENSP00000384420.1:p.Pro436=
ENST00000528996.1:c.380C>G	ENSP00000431226.1:n.380C>G
ENST00000530113.1:n.636C>G
ENST00000531133.5:c.680C>G	ENSP00000435431.1:n.680C>G
ENST00000531797.5:c.*204C>G	ENSP00000432554.1:n.*204C>G
ENST00000619430.1:c.349-39C>G	ENSP00000478572.1:n.349-39C>G
NM_000062.2:c.1179C>G , LRG_105t1:c.1179C>G	NP_000053.2:p.Pro393=
NM_001032295.1:c.1179C>G	NP_001027466.1:p.Pro393=
NM_000062.3:c.1179C>G MANE Select	NP_000053.2:p.Pro393=
NM_001032295.2:c.1179C>G	NP_001027466.1:p.Pro393=