Canonical Allele Identifier: CA380703406

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379371C>A (hg19) ; chr11:g.57611898C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611898C>A , CM000673.2:g.57611898C>A	GRCh38
NC_000011.9:g.57379371C>A , CM000673.1:g.57379371C>A	GRCh37
NC_000011.8:g.57135947C>A	NCBI36
NG_009625.1:g.19345C>A , LRG_105:g.19345C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1211C>A MANE Select	ENSP00000278407.4:p.Thr404Lys
ENST00000528996.2:c.*108C>A	ENSP00000431226.2:n.*108C>A
ENST00000531605.2:c.*987C>A	ENSP00000503752.1:n.*987C>A
ENST00000619430.2:c.1007C>A	ENSP00000478572.2:p.Thr336Lys
ENST00000676670.1:c.1211C>A	ENSP00000504807.1:p.Thr404Lys
ENST00000676741.1:n.2293C>A
ENST00000677624.1:c.*631C>A	ENSP00000503979.1:n.*631C>A
ENST00000677625.1:c.1157C>A	ENSP00000502857.1:p.Thr386Lys
ENST00000677856.1:n.1464C>A
ENST00000677915.1:c.*108C>A	ENSP00000503118.1:n.*108C>A
ENST00000678533.1:c.*765C>A	ENSP00000503873.1:n.*765C>A
ENST00000678592.1:c.*151C>A	ENSP00000504424.1:n.*151C>A
ENST00000278407.8:c.1211C>A	ENSP00000278407.4:p.Thr404Lys
ENST00000340687.10:c.1100C>A	ENSP00000341861.6:p.Thr367Lys
ENST00000378323.8:c.1226C>A	ENSP00000367574.4:p.Thr409Lys
ENST00000378324.6:c.1055C>A	ENSP00000367575.2:p.Thr352Lys
ENST00000403558.1:c.1340C>A	ENSP00000384420.1:p.Thr447Lys
ENST00000528996.1:c.412C>A	ENSP00000431226.1:n.412C>A
ENST00000530113.1:n.668C>A
ENST00000531133.5:c.712C>A	ENSP00000435431.1:n.712C>A
ENST00000531797.5:c.*236C>A	ENSP00000432554.1:n.*236C>A
ENST00000619430.1:c.349-7C>A	ENSP00000478572.1:n.349-7C>A
NM_000062.2:c.1211C>A , LRG_105t1:c.1211C>A	NP_000053.2:p.Thr404Lys
NM_001032295.1:c.1211C>A	NP_001027466.1:p.Thr404Lys
NM_000062.3:c.1211C>A MANE Select	NP_000053.2:p.Thr404Lys
NM_001032295.2:c.1211C>A	NP_001027466.1:p.Thr404Lys