Canonical Allele Identifier: CA380698495

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373485C>A (hg19) ; chr11:g.57606012C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606012C>A , CM000673.2:g.57606012C>A	GRCh38
NC_000011.9:g.57373485C>A , CM000673.1:g.57373485C>A	GRCh37
NC_000011.8:g.57130061C>A	NCBI36
NG_009625.1:g.13459C>A , LRG_105:g.13459C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.688C>A MANE Select	ENSP00000278407.4:p.Leu230Met
ENST00000528996.2:c.59-5714C>A	ENSP00000431226.2:n.59-5714C>A
ENST00000531605.2:c.*464C>A	ENSP00000503752.1:n.*464C>A
ENST00000619430.2:c.686-396C>A	ENSP00000478572.2:n.686-396C>A
ENST00000676670.1:c.688C>A	ENSP00000504807.1:p.Leu230Met
ENST00000676741.1:n.1770C>A
ENST00000677624.1:c.*108C>A	ENSP00000503979.1:n.*108C>A
ENST00000677625.1:c.688C>A	ENSP00000502857.1:p.Leu230Met
ENST00000677856.1:n.747C>A
ENST00000677915.1:c.685+3843C>A	ENSP00000503118.1:n.685+3843C>A
ENST00000678533.1:c.*242C>A	ENSP00000503873.1:n.*242C>A
ENST00000678592.1:c.688C>A	ENSP00000504424.1:p.Leu230Met
ENST00000278407.8:c.688C>A	ENSP00000278407.4:p.Leu230Met
ENST00000340687.10:c.688C>A	ENSP00000341861.6:p.Leu230Met
ENST00000378323.8:c.703C>A	ENSP00000367574.4:p.Leu235Met
ENST00000378324.6:c.532C>A	ENSP00000367575.2:p.Leu178Met
ENST00000403558.1:c.790C>A	ENSP00000384420.1:p.Leu264Met
ENST00000531133.5:c.189C>A	ENSP00000435431.1:n.189C>A
ENST00000531605.1:n.535C>A
ENST00000531797.5:c.*54+3843C>A	ENSP00000432554.1:n.*54+3843C>A
ENST00000619430.1:c.348+5837C>A	ENSP00000478572.1:n.348+5837C>A
NM_000062.2:c.688C>A , LRG_105t1:c.688C>A	NP_000053.2:p.Leu230Met
NM_001032295.1:c.688C>A	NP_001027466.1:p.Leu230Met
NM_000062.3:c.688C>A MANE Select	NP_000053.2:p.Leu230Met
NM_001032295.2:c.688C>A	NP_001027466.1:p.Leu230Met