Canonical Allele Identifier: CA380703196

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379335A>G (hg19) ; chr11:g.57611862A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611862A>G , CM000673.2:g.57611862A>G	GRCh38
NC_000011.9:g.57379335A>G , CM000673.1:g.57379335A>G	GRCh37
NC_000011.8:g.57135911A>G	NCBI36
NG_009625.1:g.19309A>G , LRG_105:g.19309A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1175A>G MANE Select	ENSP00000278407.4:p.Gln392Arg
ENST00000528996.2:c.*72A>G	ENSP00000431226.2:n.*72A>G
ENST00000531605.2:c.*951A>G	ENSP00000503752.1:n.*951A>G
ENST00000619430.2:c.971A>G	ENSP00000478572.2:p.Gln324Arg
ENST00000676670.1:c.1175A>G	ENSP00000504807.1:p.Gln392Arg
ENST00000676741.1:n.2257A>G
ENST00000677624.1:c.*595A>G	ENSP00000503979.1:n.*595A>G
ENST00000677625.1:c.1121A>G	ENSP00000502857.1:p.Gln374Arg
ENST00000677856.1:n.1428A>G
ENST00000677915.1:c.*72A>G	ENSP00000503118.1:n.*72A>G
ENST00000678533.1:c.*729A>G	ENSP00000503873.1:n.*729A>G
ENST00000678592.1:c.*115A>G	ENSP00000504424.1:n.*115A>G
ENST00000278407.8:c.1175A>G	ENSP00000278407.4:p.Gln392Arg
ENST00000340687.10:c.1064A>G	ENSP00000341861.6:p.Gln355Arg
ENST00000378323.8:c.1190A>G	ENSP00000367574.4:p.Gln397Arg
ENST00000378324.6:c.1019A>G	ENSP00000367575.2:p.Gln340Arg
ENST00000403558.1:c.1304A>G	ENSP00000384420.1:p.Gln435Arg
ENST00000528996.1:c.376A>G	ENSP00000431226.1:n.376A>G
ENST00000530113.1:n.632A>G
ENST00000531133.5:c.676A>G	ENSP00000435431.1:n.676A>G
ENST00000531797.5:c.*200A>G	ENSP00000432554.1:n.*200A>G
ENST00000619430.1:c.349-43A>G	ENSP00000478572.1:n.349-43A>G
NM_000062.2:c.1175A>G , LRG_105t1:c.1175A>G	NP_000053.2:p.Gln392Arg
NM_001032295.1:c.1175A>G	NP_001027466.1:p.Gln392Arg
NM_000062.3:c.1175A>G MANE Select	NP_000053.2:p.Gln392Arg
NM_001032295.2:c.1175A>G	NP_001027466.1:p.Gln392Arg