Canonical Allele Identifier: CA380702554

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379239C>G (hg19) ; chr11:g.57611766C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611766C>G , CM000673.2:g.57611766C>G	GRCh38
NC_000011.9:g.57379239C>G , CM000673.1:g.57379239C>G	GRCh37
NC_000011.8:g.57135815C>G	NCBI36
NG_009625.1:g.19213C>G , LRG_105:g.19213C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1079C>G MANE Select	ENSP00000278407.4:p.Pro360Arg
ENST00000528996.2:c.99C>G	ENSP00000431226.2:p.Thr33=
ENST00000531605.2:c.*855C>G	ENSP00000503752.1:n.*855C>G
ENST00000619430.2:c.875C>G	ENSP00000478572.2:p.Pro292Arg
ENST00000676670.1:c.1079C>G	ENSP00000504807.1:p.Pro360Arg
ENST00000676741.1:n.2161C>G
ENST00000677624.1:c.*499C>G	ENSP00000503979.1:n.*499C>G
ENST00000677625.1:c.1030-5C>G	ENSP00000502857.1:n.1030-5C>G
ENST00000677856.1:n.1332C>G
ENST00000677915.1:c.735C>G	ENSP00000503118.1:p.Thr245=
ENST00000678533.1:c.*633C>G	ENSP00000503873.1:n.*633C>G
ENST00000678592.1:c.*19C>G	ENSP00000504424.1:n.*19C>G
ENST00000278407.8:c.1079C>G	ENSP00000278407.4:p.Pro360Arg
ENST00000340687.10:c.1030-62C>G	ENSP00000341861.6:n.1030-62C>G
ENST00000378323.8:c.1094C>G	ENSP00000367574.4:p.Pro365Arg
ENST00000378324.6:c.923C>G	ENSP00000367575.2:p.Pro308Arg
ENST00000403558.1:c.1208C>G	ENSP00000384420.1:p.Pro403Arg
ENST00000528996.1:c.280C>G	ENSP00000431226.1:n.280C>G
ENST00000530113.1:n.536C>G
ENST00000531133.5:c.580C>G	ENSP00000435431.1:n.580C>G
ENST00000531797.5:c.*104C>G	ENSP00000432554.1:n.*104C>G
ENST00000619430.1:c.349-139C>G	ENSP00000478572.1:n.349-139C>G
NM_000062.2:c.1079C>G , LRG_105t1:c.1079C>G	NP_000053.2:p.Pro360Arg
NM_001032295.1:c.1079C>G	NP_001027466.1:p.Pro360Arg
NM_000062.3:c.1079C>G MANE Select	NP_000053.2:p.Pro360Arg
NM_001032295.2:c.1079C>G	NP_001027466.1:p.Pro360Arg