Canonical Allele Identifier: CA380702601

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379245A>T (hg19) ; chr11:g.57611772A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611772A>T , CM000673.2:g.57611772A>T	GRCh38
NC_000011.9:g.57379245A>T , CM000673.1:g.57379245A>T	GRCh37
NC_000011.8:g.57135821A>T	NCBI36
NG_009625.1:g.19219A>T , LRG_105:g.19219A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1085A>T MANE Select	ENSP00000278407.4:p.Asn362Ile
ENST00000528996.2:c.105A>T	ENSP00000431226.2:p.Glu35Asp
ENST00000531605.2:c.*861A>T	ENSP00000503752.1:n.*861A>T
ENST00000619430.2:c.881A>T	ENSP00000478572.2:p.Asn294Ile
ENST00000676670.1:c.1085A>T	ENSP00000504807.1:p.Asn362Ile
ENST00000676741.1:n.2167A>T
ENST00000677624.1:c.*505A>T	ENSP00000503979.1:n.*505A>T
ENST00000677625.1:c.1031A>T	ENSP00000502857.1:p.Asn344Ile
ENST00000677856.1:n.1338A>T
ENST00000677915.1:c.741A>T	ENSP00000503118.1:p.Glu247Asp
ENST00000678533.1:c.*639A>T	ENSP00000503873.1:n.*639A>T
ENST00000678592.1:c.*25A>T	ENSP00000504424.1:n.*25A>T
ENST00000278407.8:c.1085A>T	ENSP00000278407.4:p.Asn362Ile
ENST00000340687.10:c.1030-56A>T	ENSP00000341861.6:n.1030-56A>T
ENST00000378323.8:c.1100A>T	ENSP00000367574.4:p.Asn367Ile
ENST00000378324.6:c.929A>T	ENSP00000367575.2:p.Asn310Ile
ENST00000403558.1:c.1214A>T	ENSP00000384420.1:p.Asn405Ile
ENST00000528996.1:c.286A>T	ENSP00000431226.1:n.286A>T
ENST00000530113.1:n.542A>T
ENST00000531133.5:c.586A>T	ENSP00000435431.1:n.586A>T
ENST00000531797.5:c.*110A>T	ENSP00000432554.1:n.*110A>T
ENST00000619430.1:c.349-133A>T	ENSP00000478572.1:n.349-133A>T
NM_000062.2:c.1085A>T , LRG_105t1:c.1085A>T	NP_000053.2:p.Asn362Ile
NM_001032295.1:c.1085A>T	NP_001027466.1:p.Asn362Ile
NM_000062.3:c.1085A>T MANE Select	NP_000053.2:p.Asn362Ile
NM_001032295.2:c.1085A>T	NP_001027466.1:p.Asn362Ile