Canonical Allele Identifier: CA380690801

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381977C>G (hg19) ; chr11:g.57614504C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614504C>G , CM000673.2:g.57614504C>G	GRCh38
NC_000011.9:g.57381977C>G , CM000673.1:g.57381977C>G	GRCh37
NC_000011.8:g.57138553C>G	NCBI36
NG_009625.1:g.21951C>G , LRG_105:g.21951C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1426C>G MANE Select	ENSP00000278407.4:p.Pro476Ala
ENST00000528996.2:c.*323C>G	ENSP00000431226.2:n.*323C>G
ENST00000531605.2:c.*1202C>G	ENSP00000503752.1:n.*1202C>G
ENST00000619430.2:c.1222C>G	ENSP00000478572.2:p.Pro408Ala
ENST00000676670.1:c.1426C>G	ENSP00000504807.1:p.Pro476Ala
ENST00000676741.1:n.2508C>G
ENST00000677624.1:c.*846C>G	ENSP00000503979.1:n.*846C>G
ENST00000677625.1:c.1372C>G	ENSP00000502857.1:p.Pro458Ala
ENST00000677856.1:n.1679C>G
ENST00000677915.1:c.*323C>G	ENSP00000503118.1:n.*323C>G
ENST00000678533.1:c.*980C>G	ENSP00000503873.1:n.*980C>G
ENST00000678592.1:c.*366C>G	ENSP00000504424.1:n.*366C>G
ENST00000278407.8:c.1426C>G	ENSP00000278407.4:p.Pro476Ala
ENST00000340687.10:c.1315C>G	ENSP00000341861.6:p.Pro439Ala
ENST00000378323.8:c.1441C>G	ENSP00000367574.4:p.Pro481Ala
ENST00000378324.6:c.1270C>G	ENSP00000367575.2:p.Pro424Ala
ENST00000403558.1:c.1555C>G	ENSP00000384420.1:p.Pro519Ala
ENST00000528996.1:c.627C>G	ENSP00000431226.1:n.627C>G
ENST00000530113.1:n.883C>G
ENST00000531133.5:c.927C>G	ENSP00000435431.1:n.927C>G
ENST00000531797.5:c.*451C>G	ENSP00000432554.1:n.*451C>G
ENST00000619430.1:c.557C>G	ENSP00000478572.1:n.557C>G
NM_000062.2:c.1426C>G , LRG_105t1:c.1426C>G	NP_000053.2:p.Pro476Ala
NM_001032295.1:c.1426C>G	NP_001027466.1:p.Pro476Ala
NM_000062.3:c.1426C>G MANE Select	NP_000053.2:p.Pro476Ala
NM_001032295.2:c.1426C>G	NP_001027466.1:p.Pro476Ala