Canonical Allele Identifier: CA474806929

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381991G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614518G>A , CM000673.2:g.57614518G>A	GRCh38
NC_000011.9:g.57381991G>A , CM000673.1:g.57381991G>A	GRCh37
NC_000011.8:g.57138567G>A	NCBI36
NG_009625.1:g.21965G>A , LRG_105:g.21965G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1440G>A MANE Select	ENSP00000278407.4:p.Val480=
ENST00000528996.2:c.*337G>A	ENSP00000431226.2:n.*337G>A
ENST00000531605.2:c.*1216G>A	ENSP00000503752.1:n.*1216G>A
ENST00000619430.2:c.1236G>A	ENSP00000478572.2:p.Val412=
ENST00000676670.1:c.1440G>A	ENSP00000504807.1:p.Val480=
ENST00000676741.1:n.2522G>A
ENST00000677624.1:c.*860G>A	ENSP00000503979.1:n.*860G>A
ENST00000677625.1:c.1386G>A	ENSP00000502857.1:p.Val462=
ENST00000677856.1:n.1693G>A
ENST00000677915.1:c.*337G>A	ENSP00000503118.1:n.*337G>A
ENST00000678533.1:c.*994G>A	ENSP00000503873.1:n.*994G>A
ENST00000678592.1:c.*380G>A	ENSP00000504424.1:n.*380G>A
ENST00000278407.8:c.1440G>A	ENSP00000278407.4:p.Val480=
ENST00000340687.10:c.1329G>A	ENSP00000341861.6:p.Val443=
ENST00000378323.8:c.1455G>A	ENSP00000367574.4:p.Val485=
ENST00000378324.6:c.1284G>A	ENSP00000367575.2:p.Val428=
ENST00000403558.1:c.1569G>A	ENSP00000384420.1:p.Val523=
ENST00000528996.1:c.641G>A	ENSP00000431226.1:n.641G>A
ENST00000530113.1:n.897G>A
ENST00000531133.5:c.941G>A	ENSP00000435431.1:n.941G>A
ENST00000531797.5:c.*465G>A	ENSP00000432554.1:n.*465G>A
ENST00000619430.1:c.571G>A	ENSP00000478572.1:n.571G>A
NM_000062.2:c.1440G>A , LRG_105t1:c.1440G>A	NP_000053.2:p.Val480=
NM_001032295.1:c.1440G>A	NP_001027466.1:p.Val480=
NM_000062.3:c.1440G>A MANE Select	NP_000053.2:p.Val480=
NM_001032295.2:c.1440G>A	NP_001027466.1:p.Val480=