Canonical Allele Identifier: CA380690201

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381815T>A (hg19) ; chr11:g.57614342T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614342T>A , CM000673.2:g.57614342T>A	GRCh38
NC_000011.9:g.57381815T>A , CM000673.1:g.57381815T>A	GRCh37
NC_000011.8:g.57138391T>A	NCBI36
NG_009625.1:g.21789T>A , LRG_105:g.21789T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1264T>A MANE Select	ENSP00000278407.4:p.Ser422Thr
ENST00000528996.2:c.*161T>A	ENSP00000431226.2:n.*161T>A
ENST00000531605.2:c.*1040T>A	ENSP00000503752.1:n.*1040T>A
ENST00000619430.2:c.1060T>A	ENSP00000478572.2:p.Ser354Thr
ENST00000676670.1:c.1264T>A	ENSP00000504807.1:p.Ser422Thr
ENST00000676741.1:n.2346T>A
ENST00000677624.1:c.*684T>A	ENSP00000503979.1:n.*684T>A
ENST00000677625.1:c.1210T>A	ENSP00000502857.1:p.Ser404Thr
ENST00000677856.1:n.1517T>A
ENST00000677915.1:c.*161T>A	ENSP00000503118.1:n.*161T>A
ENST00000678533.1:c.*818T>A	ENSP00000503873.1:n.*818T>A
ENST00000678592.1:c.*204T>A	ENSP00000504424.1:n.*204T>A
ENST00000278407.8:c.1264T>A	ENSP00000278407.4:p.Ser422Thr
ENST00000340687.10:c.1153T>A	ENSP00000341861.6:p.Ser385Thr
ENST00000378323.8:c.1279T>A	ENSP00000367574.4:p.Ser427Thr
ENST00000378324.6:c.1108T>A	ENSP00000367575.2:p.Ser370Thr
ENST00000403558.1:c.1393T>A	ENSP00000384420.1:p.Ser465Thr
ENST00000528996.1:c.465T>A	ENSP00000431226.1:n.465T>A
ENST00000530113.1:n.721T>A
ENST00000531133.5:c.765T>A	ENSP00000435431.1:n.765T>A
ENST00000531797.5:c.*289T>A	ENSP00000432554.1:n.*289T>A
ENST00000619430.1:c.395T>A	ENSP00000478572.1:p.Phe132Tyr
NM_000062.2:c.1264T>A , LRG_105t1:c.1264T>A	NP_000053.2:p.Ser422Thr
NM_001032295.1:c.1264T>A	NP_001027466.1:p.Ser422Thr
NM_000062.3:c.1264T>A MANE Select	NP_000053.2:p.Ser422Thr
NM_001032295.2:c.1264T>A	NP_001027466.1:p.Ser422Thr