Canonical Allele Identifier: CA474806867

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381946C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614473C>A , CM000673.2:g.57614473C>A	GRCh38
NC_000011.9:g.57381946C>A , CM000673.1:g.57381946C>A	GRCh37
NC_000011.8:g.57138522C>A	NCBI36
NG_009625.1:g.21920C>A , LRG_105:g.21920C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1395C>A MANE Select	ENSP00000278407.4:p.Ala465=
ENST00000528996.2:c.*292C>A	ENSP00000431226.2:n.*292C>A
ENST00000531605.2:c.*1171C>A	ENSP00000503752.1:n.*1171C>A
ENST00000619430.2:c.1191C>A	ENSP00000478572.2:p.Ala397=
ENST00000676670.1:c.1395C>A	ENSP00000504807.1:p.Ala465=
ENST00000676741.1:n.2477C>A
ENST00000677624.1:c.*815C>A	ENSP00000503979.1:n.*815C>A
ENST00000677625.1:c.1341C>A	ENSP00000502857.1:p.Ala447=
ENST00000677856.1:n.1648C>A
ENST00000677915.1:c.*292C>A	ENSP00000503118.1:n.*292C>A
ENST00000678533.1:c.*949C>A	ENSP00000503873.1:n.*949C>A
ENST00000678592.1:c.*335C>A	ENSP00000504424.1:n.*335C>A
ENST00000278407.8:c.1395C>A	ENSP00000278407.4:p.Ala465=
ENST00000340687.10:c.1284C>A	ENSP00000341861.6:p.Ala428=
ENST00000378323.8:c.1410C>A	ENSP00000367574.4:p.Ala470=
ENST00000378324.6:c.1239C>A	ENSP00000367575.2:p.Ala413=
ENST00000403558.1:c.1524C>A	ENSP00000384420.1:p.Ala508=
ENST00000528996.1:c.596C>A	ENSP00000431226.1:n.596C>A
ENST00000530113.1:n.852C>A
ENST00000531133.5:c.896C>A	ENSP00000435431.1:n.896C>A
ENST00000531797.5:c.*420C>A	ENSP00000432554.1:n.*420C>A
ENST00000619430.1:c.526C>A	ENSP00000478572.1:n.526C>A
NM_000062.2:c.1395C>A , LRG_105t1:c.1395C>A	NP_000053.2:p.Ala465=
NM_001032295.1:c.1395C>A	NP_001027466.1:p.Ala465=
NM_000062.3:c.1395C>A MANE Select	NP_000053.2:p.Ala465=
NM_001032295.2:c.1395C>A	NP_001027466.1:p.Ala465=