Canonical Allele Identifier: CA380699758

Gene: SERPING1

Linked Data

• COSMIC: COSM4197543
• MyVariant Identifiers: chr11:g.57373672C>A (hg19) ; chr11:g.57606199C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606199C>A , CM000673.2:g.57606199C>A	GRCh38
NC_000011.9:g.57373672C>A , CM000673.1:g.57373672C>A	GRCh37
NC_000011.8:g.57130248C>A	NCBI36
NG_009625.1:g.13646C>A , LRG_105:g.13646C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.875C>A MANE Select	ENSP00000278407.4:p.Ala292Asp
ENST00000528996.2:c.59-5527C>A	ENSP00000431226.2:n.59-5527C>A
ENST00000531605.2:c.*651C>A	ENSP00000503752.1:n.*651C>A
ENST00000619430.2:c.686-209C>A	ENSP00000478572.2:n.686-209C>A
ENST00000676670.1:c.875C>A	ENSP00000504807.1:p.Ala292Asp
ENST00000676741.1:n.1957C>A
ENST00000677624.1:c.*295C>A	ENSP00000503979.1:n.*295C>A
ENST00000677625.1:c.875C>A	ENSP00000502857.1:p.Ala292Asp
ENST00000677856.1:n.934C>A
ENST00000677915.1:c.685+4030C>A	ENSP00000503118.1:n.685+4030C>A
ENST00000678533.1:c.*429C>A	ENSP00000503873.1:n.*429C>A
ENST00000678592.1:c.875C>A	ENSP00000504424.1:p.Ala292Asp
ENST00000278407.8:c.875C>A	ENSP00000278407.4:p.Ala292Asp
ENST00000340687.10:c.875C>A	ENSP00000341861.6:p.Ala292Asp
ENST00000378323.8:c.890C>A	ENSP00000367574.4:p.Ala297Asp
ENST00000378324.6:c.719C>A	ENSP00000367575.2:p.Ala240Asp
ENST00000403558.1:c.977C>A	ENSP00000384420.1:p.Ala326Asp
ENST00000531133.5:c.376C>A	ENSP00000435431.1:n.376C>A
ENST00000531797.5:c.*54+4030C>A	ENSP00000432554.1:n.*54+4030C>A
ENST00000619430.1:c.349-5706C>A	ENSP00000478572.1:n.349-5706C>A
NM_000062.2:c.875C>A , LRG_105t1:c.875C>A	NP_000053.2:p.Ala292Asp
NM_001032295.1:c.875C>A	NP_001027466.1:p.Ala292Asp
NM_000062.3:c.875C>A MANE Select	NP_000053.2:p.Ala292Asp
NM_001032295.2:c.875C>A	NP_001027466.1:p.Ala292Asp