Canonical Allele Identifier: CA380703351

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611883C>G , CM000673.2:g.57611883C>G	GRCh38
NC_000011.9:g.57379356C>G , CM000673.1:g.57379356C>G	GRCh37
NC_000011.8:g.57135932C>G	NCBI36
NG_009625.1:g.19330C>G , LRG_105:g.19330C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1196C>G MANE Select	NP_000053.2:p.Pro399Arg
ENST00000278407.9:c.1196C>G MANE Select	ENSP00000278407.4:p.Pro399Arg
NM_000062.2:c.1196C>G , LRG_105t1:c.1196C>G	NP_000053.2:p.Pro399Arg
NM_001032295.1:c.1196C>G	NP_001027466.1:p.Pro399Arg
NM_001032295.2:c.1196C>G	NP_001027466.1:p.Pro399Arg
ENST00000278407.8:c.1196C>G	ENSP00000278407.4:p.Pro399Arg
ENST00000340687.10:c.1085C>G	ENSP00000341861.6:p.Pro362Arg
ENST00000378323.8:c.1211C>G	ENSP00000367574.4:p.Pro404Arg
ENST00000378324.6:c.1040C>G	ENSP00000367575.2:p.Pro347Arg
ENST00000403558.1:c.1325C>G	ENSP00000384420.1:p.Pro442Arg
ENST00000528996.1:c.397C>G	ENSP00000431226.1:n.397C>G
ENST00000528996.2:c.*93C>G	ENSP00000431226.2:n.*93C>G
ENST00000530113.1:n.653C>G
ENST00000531133.5:c.697C>G	ENSP00000435431.1:n.697C>G
ENST00000531605.2:c.*972C>G	ENSP00000503752.1:n.*972C>G
ENST00000531797.5:c.*221C>G	ENSP00000432554.1:n.*221C>G
ENST00000619430.1:c.349-22C>G	ENSP00000478572.1:n.349-22C>G
ENST00000619430.2:c.992C>G	ENSP00000478572.2:p.Pro331Arg
ENST00000676670.1:c.1196C>G	ENSP00000504807.1:p.Pro399Arg
ENST00000676741.1:n.2278C>G
ENST00000677624.1:c.*616C>G	ENSP00000503979.1:n.*616C>G
ENST00000677625.1:c.1142C>G	ENSP00000502857.1:p.Pro381Arg
ENST00000677856.1:n.1449C>G
ENST00000677915.1:c.*93C>G	ENSP00000503118.1:n.*93C>G
ENST00000678533.1:c.*750C>G	ENSP00000503873.1:n.*750C>G
ENST00000678592.1:c.*136C>G	ENSP00000504424.1:n.*136C>G