Canonical Allele Identifier: CA380702880

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379296T>A (hg19) ; chr11:g.57611823T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611823T>A , CM000673.2:g.57611823T>A	GRCh38
NC_000011.9:g.57379296T>A , CM000673.1:g.57379296T>A	GRCh37
NC_000011.8:g.57135872T>A	NCBI36
NG_009625.1:g.19270T>A , LRG_105:g.19270T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1136T>A MANE Select	ENSP00000278407.4:p.Phe379Tyr
ENST00000528996.2:c.*33T>A	ENSP00000431226.2:n.*33T>A
ENST00000531605.2:c.*912T>A	ENSP00000503752.1:n.*912T>A
ENST00000619430.2:c.932T>A	ENSP00000478572.2:p.Phe311Tyr
ENST00000676670.1:c.1136T>A	ENSP00000504807.1:p.Phe379Tyr
ENST00000676741.1:n.2218T>A
ENST00000677624.1:c.*556T>A	ENSP00000503979.1:n.*556T>A
ENST00000677625.1:c.1082T>A	ENSP00000502857.1:p.Phe361Tyr
ENST00000677856.1:n.1389T>A
ENST00000677915.1:c.*33T>A	ENSP00000503118.1:n.*33T>A
ENST00000678533.1:c.*690T>A	ENSP00000503873.1:n.*690T>A
ENST00000678592.1:c.*76T>A	ENSP00000504424.1:n.*76T>A
ENST00000278407.8:c.1136T>A	ENSP00000278407.4:p.Phe379Tyr
ENST00000340687.10:c.1030-5T>A	ENSP00000341861.6:n.1030-5T>A
ENST00000378323.8:c.1151T>A	ENSP00000367574.4:p.Phe384Tyr
ENST00000378324.6:c.980T>A	ENSP00000367575.2:p.Phe327Tyr
ENST00000403558.1:c.1265T>A	ENSP00000384420.1:p.Phe422Tyr
ENST00000528996.1:c.337T>A	ENSP00000431226.1:n.337T>A
ENST00000530113.1:n.593T>A
ENST00000531133.5:c.637T>A	ENSP00000435431.1:n.637T>A
ENST00000531797.5:c.*161T>A	ENSP00000432554.1:n.*161T>A
ENST00000619430.1:c.349-82T>A	ENSP00000478572.1:n.349-82T>A
NM_000062.2:c.1136T>A , LRG_105t1:c.1136T>A	NP_000053.2:p.Phe379Tyr
NM_001032295.1:c.1136T>A	NP_001027466.1:p.Phe379Tyr
NM_000062.3:c.1136T>A MANE Select	NP_000053.2:p.Phe379Tyr
NM_001032295.2:c.1136T>A	NP_001027466.1:p.Phe379Tyr