Canonical Allele Identifier: CA380699540

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373634C>A (hg19) ; chr11:g.57606161C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606161C>A , CM000673.2:g.57606161C>A	GRCh38
NC_000011.9:g.57373634C>A , CM000673.1:g.57373634C>A	GRCh37
NC_000011.8:g.57130210C>A	NCBI36
NG_009625.1:g.13608C>A , LRG_105:g.13608C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.837C>A MANE Select	ENSP00000278407.4:p.Asp279Glu
ENST00000528996.2:c.59-5565C>A	ENSP00000431226.2:n.59-5565C>A
ENST00000531605.2:c.*613C>A	ENSP00000503752.1:n.*613C>A
ENST00000619430.2:c.686-247C>A	ENSP00000478572.2:n.686-247C>A
ENST00000676670.1:c.837C>A	ENSP00000504807.1:p.Asp279Glu
ENST00000676741.1:n.1919C>A
ENST00000677624.1:c.*257C>A	ENSP00000503979.1:n.*257C>A
ENST00000677625.1:c.837C>A	ENSP00000502857.1:p.Asp279Glu
ENST00000677856.1:n.896C>A
ENST00000677915.1:c.685+3992C>A	ENSP00000503118.1:n.685+3992C>A
ENST00000678533.1:c.*391C>A	ENSP00000503873.1:n.*391C>A
ENST00000678592.1:c.837C>A	ENSP00000504424.1:p.Asp279Glu
ENST00000278407.8:c.837C>A	ENSP00000278407.4:p.Asp279Glu
ENST00000340687.10:c.837C>A	ENSP00000341861.6:p.Asp279Glu
ENST00000378323.8:c.852C>A	ENSP00000367574.4:p.Asp284Glu
ENST00000378324.6:c.681C>A	ENSP00000367575.2:p.Asp227Glu
ENST00000403558.1:c.939C>A	ENSP00000384420.1:p.Asp313Glu
ENST00000531133.5:c.338C>A	ENSP00000435431.1:n.338C>A
ENST00000531797.5:c.*54+3992C>A	ENSP00000432554.1:n.*54+3992C>A
ENST00000619430.1:c.349-5744C>A	ENSP00000478572.1:n.349-5744C>A
NM_000062.2:c.837C>A , LRG_105t1:c.837C>A	NP_000053.2:p.Asp279Glu
NM_001032295.1:c.837C>A	NP_001027466.1:p.Asp279Glu
NM_000062.3:c.837C>A MANE Select	NP_000053.2:p.Asp279Glu
NM_001032295.2:c.837C>A	NP_001027466.1:p.Asp279Glu