Canonical Allele Identifier: CA380702616

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379248T>A (hg19) ; chr11:g.57611775T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611775T>A , CM000673.2:g.57611775T>A	GRCh38
NC_000011.9:g.57379248T>A , CM000673.1:g.57379248T>A	GRCh37
NC_000011.8:g.57135824T>A	NCBI36
NG_009625.1:g.19222T>A , LRG_105:g.19222T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1088T>A MANE Select	ENSP00000278407.4:p.Leu363Gln
ENST00000528996.2:c.108T>A	ENSP00000431226.2:p.Pro36=
ENST00000531605.2:c.*864T>A	ENSP00000503752.1:n.*864T>A
ENST00000619430.2:c.884T>A	ENSP00000478572.2:p.Leu295Gln
ENST00000676670.1:c.1088T>A	ENSP00000504807.1:p.Leu363Gln
ENST00000676741.1:n.2170T>A
ENST00000677624.1:c.*508T>A	ENSP00000503979.1:n.*508T>A
ENST00000677625.1:c.1034T>A	ENSP00000502857.1:p.Leu345Gln
ENST00000677856.1:n.1341T>A
ENST00000677915.1:c.744T>A	ENSP00000503118.1:p.Pro248=
ENST00000678533.1:c.*642T>A	ENSP00000503873.1:n.*642T>A
ENST00000678592.1:c.*28T>A	ENSP00000504424.1:n.*28T>A
ENST00000278407.8:c.1088T>A	ENSP00000278407.4:p.Leu363Gln
ENST00000340687.10:c.1030-53T>A	ENSP00000341861.6:n.1030-53T>A
ENST00000378323.8:c.1103T>A	ENSP00000367574.4:p.Leu368Gln
ENST00000378324.6:c.932T>A	ENSP00000367575.2:p.Leu311Gln
ENST00000403558.1:c.1217T>A	ENSP00000384420.1:p.Leu406Gln
ENST00000528996.1:c.289T>A	ENSP00000431226.1:n.289T>A
ENST00000530113.1:n.545T>A
ENST00000531133.5:c.589T>A	ENSP00000435431.1:n.589T>A
ENST00000531797.5:c.*113T>A	ENSP00000432554.1:n.*113T>A
ENST00000619430.1:c.349-130T>A	ENSP00000478572.1:n.349-130T>A
NM_000062.2:c.1088T>A , LRG_105t1:c.1088T>A	NP_000053.2:p.Leu363Gln
NM_001032295.1:c.1088T>A	NP_001027466.1:p.Leu363Gln
NM_000062.3:c.1088T>A MANE Select	NP_000053.2:p.Leu363Gln
NM_001032295.2:c.1088T>A	NP_001027466.1:p.Leu363Gln