Canonical Allele Identifier: CA380702648

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379253C>A (hg19) ; chr11:g.57611780C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611780C>A , CM000673.2:g.57611780C>A	GRCh38
NC_000011.9:g.57379253C>A , CM000673.1:g.57379253C>A	GRCh37
NC_000011.8:g.57135829C>A	NCBI36
NG_009625.1:g.19227C>A , LRG_105:g.19227C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1093C>A MANE Select	ENSP00000278407.4:p.His365Asn
ENST00000528996.2:c.113C>A	ENSP00000431226.2:p.Thr38Lys
ENST00000531605.2:c.*869C>A	ENSP00000503752.1:n.*869C>A
ENST00000619430.2:c.889C>A	ENSP00000478572.2:p.His297Asn
ENST00000676670.1:c.1093C>A	ENSP00000504807.1:p.His365Asn
ENST00000676741.1:n.2175C>A
ENST00000677624.1:c.*513C>A	ENSP00000503979.1:n.*513C>A
ENST00000677625.1:c.1039C>A	ENSP00000502857.1:p.His347Asn
ENST00000677856.1:n.1346C>A
ENST00000677915.1:c.749C>A	ENSP00000503118.1:p.Thr250Lys
ENST00000678533.1:c.*647C>A	ENSP00000503873.1:n.*647C>A
ENST00000678592.1:c.*33C>A	ENSP00000504424.1:n.*33C>A
ENST00000278407.8:c.1093C>A	ENSP00000278407.4:p.His365Asn
ENST00000340687.10:c.1030-48C>A	ENSP00000341861.6:n.1030-48C>A
ENST00000378323.8:c.1108C>A	ENSP00000367574.4:p.His370Asn
ENST00000378324.6:c.937C>A	ENSP00000367575.2:p.His313Asn
ENST00000403558.1:c.1222C>A	ENSP00000384420.1:p.His408Asn
ENST00000528996.1:c.294C>A	ENSP00000431226.1:n.294C>A
ENST00000530113.1:n.550C>A
ENST00000531133.5:c.594C>A	ENSP00000435431.1:n.594C>A
ENST00000531797.5:c.*118C>A	ENSP00000432554.1:n.*118C>A
ENST00000619430.1:c.349-125C>A	ENSP00000478572.1:n.349-125C>A
NM_000062.2:c.1093C>A , LRG_105t1:c.1093C>A	NP_000053.2:p.His365Asn
NM_001032295.1:c.1093C>A	NP_001027466.1:p.His365Asn
NM_000062.3:c.1093C>A MANE Select	NP_000053.2:p.His365Asn
NM_001032295.2:c.1093C>A	NP_001027466.1:p.His365Asn