Canonical Allele Identifier: CA380690358

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381849A>T (hg19) ; chr11:g.57614376A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614376A>T , CM000673.2:g.57614376A>T	GRCh38
NC_000011.9:g.57381849A>T , CM000673.1:g.57381849A>T	GRCh37
NC_000011.8:g.57138425A>T	NCBI36
NG_009625.1:g.21823A>T , LRG_105:g.21823A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1298A>T MANE Select	ENSP00000278407.4:p.Asp433Val
ENST00000528996.2:c.*195A>T	ENSP00000431226.2:n.*195A>T
ENST00000531605.2:c.*1074A>T	ENSP00000503752.1:n.*1074A>T
ENST00000619430.2:c.1094A>T	ENSP00000478572.2:p.Asp365Val
ENST00000676670.1:c.1298A>T	ENSP00000504807.1:p.Asp433Val
ENST00000676741.1:n.2380A>T
ENST00000677624.1:c.*718A>T	ENSP00000503979.1:n.*718A>T
ENST00000677625.1:c.1244A>T	ENSP00000502857.1:p.Asp415Val
ENST00000677856.1:n.1551A>T
ENST00000677915.1:c.*195A>T	ENSP00000503118.1:n.*195A>T
ENST00000678533.1:c.*852A>T	ENSP00000503873.1:n.*852A>T
ENST00000678592.1:c.*238A>T	ENSP00000504424.1:n.*238A>T
ENST00000278407.8:c.1298A>T	ENSP00000278407.4:p.Asp433Val
ENST00000340687.10:c.1187A>T	ENSP00000341861.6:p.Asp396Val
ENST00000378323.8:c.1313A>T	ENSP00000367574.4:p.Asp438Val
ENST00000378324.6:c.1142A>T	ENSP00000367575.2:p.Asp381Val
ENST00000403558.1:c.1427A>T	ENSP00000384420.1:p.Asp476Val
ENST00000528996.1:c.499A>T	ENSP00000431226.1:n.499A>T
ENST00000530113.1:n.755A>T
ENST00000531133.5:c.799A>T	ENSP00000435431.1:n.799A>T
ENST00000531797.5:c.*323A>T	ENSP00000432554.1:n.*323A>T
ENST00000619430.1:c.429A>T	ENSP00000478572.1:n.429A>T
NM_000062.2:c.1298A>T , LRG_105t1:c.1298A>T	NP_000053.2:p.Asp433Val
NM_001032295.1:c.1298A>T	NP_001027466.1:p.Asp433Val
NM_000062.3:c.1298A>T MANE Select	NP_000053.2:p.Asp433Val
NM_001032295.2:c.1298A>T	NP_001027466.1:p.Asp433Val