Canonical Allele Identifier: CA380699168

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373579T>A (hg19) ; chr11:g.57606106T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606106T>A , CM000673.2:g.57606106T>A	GRCh38
NC_000011.9:g.57373579T>A , CM000673.1:g.57373579T>A	GRCh37
NC_000011.8:g.57130155T>A	NCBI36
NG_009625.1:g.13553T>A , LRG_105:g.13553T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.782T>A MANE Select	ENSP00000278407.4:p.Leu261His
ENST00000528996.2:c.59-5620T>A	ENSP00000431226.2:n.59-5620T>A
ENST00000531605.2:c.*558T>A	ENSP00000503752.1:n.*558T>A
ENST00000619430.2:c.686-302T>A	ENSP00000478572.2:n.686-302T>A
ENST00000676670.1:c.782T>A	ENSP00000504807.1:p.Leu261His
ENST00000676741.1:n.1864T>A
ENST00000677624.1:c.*202T>A	ENSP00000503979.1:n.*202T>A
ENST00000677625.1:c.782T>A	ENSP00000502857.1:p.Leu261His
ENST00000677856.1:n.841T>A
ENST00000677915.1:c.685+3937T>A	ENSP00000503118.1:n.685+3937T>A
ENST00000678533.1:c.*336T>A	ENSP00000503873.1:n.*336T>A
ENST00000678592.1:c.782T>A	ENSP00000504424.1:p.Leu261His
ENST00000278407.8:c.782T>A	ENSP00000278407.4:p.Leu261His
ENST00000340687.10:c.782T>A	ENSP00000341861.6:p.Leu261His
ENST00000378323.8:c.797T>A	ENSP00000367574.4:p.Leu266His
ENST00000378324.6:c.626T>A	ENSP00000367575.2:p.Leu209His
ENST00000403558.1:c.884T>A	ENSP00000384420.1:p.Leu295His
ENST00000531133.5:c.283T>A	ENSP00000435431.1:n.283T>A
ENST00000531797.5:c.*54+3937T>A	ENSP00000432554.1:n.*54+3937T>A
ENST00000619430.1:c.349-5799T>A	ENSP00000478572.1:n.349-5799T>A
NM_000062.2:c.782T>A , LRG_105t1:c.782T>A	NP_000053.2:p.Leu261His
NM_001032295.1:c.782T>A	NP_001027466.1:p.Leu261His
NM_000062.3:c.782T>A MANE Select	NP_000053.2:p.Leu261His
NM_001032295.2:c.782T>A	NP_001027466.1:p.Leu261His