Canonical Allele Identifier: CA380702787

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379272A>C (hg19) ; chr11:g.57611799A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611799A>C , CM000673.2:g.57611799A>C	GRCh38
NC_000011.9:g.57379272A>C , CM000673.1:g.57379272A>C	GRCh37
NC_000011.8:g.57135848A>C	NCBI36
NG_009625.1:g.19246A>C , LRG_105:g.19246A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1112A>C MANE Select	ENSP00000278407.4:p.Glu371Ala
ENST00000528996.2:c.*9A>C	ENSP00000431226.2:n.*9A>C
ENST00000531605.2:c.*888A>C	ENSP00000503752.1:n.*888A>C
ENST00000619430.2:c.908A>C	ENSP00000478572.2:p.Glu303Ala
ENST00000676670.1:c.1112A>C	ENSP00000504807.1:p.Glu371Ala
ENST00000676741.1:n.2194A>C
ENST00000677624.1:c.*532A>C	ENSP00000503979.1:n.*532A>C
ENST00000677625.1:c.1058A>C	ENSP00000502857.1:p.Glu353Ala
ENST00000677856.1:n.1365A>C
ENST00000677915.1:c.*9A>C	ENSP00000503118.1:n.*9A>C
ENST00000678533.1:c.*666A>C	ENSP00000503873.1:n.*666A>C
ENST00000678592.1:c.*52A>C	ENSP00000504424.1:n.*52A>C
ENST00000278407.8:c.1112A>C	ENSP00000278407.4:p.Glu371Ala
ENST00000340687.10:c.1030-29A>C	ENSP00000341861.6:n.1030-29A>C
ENST00000378323.8:c.1127A>C	ENSP00000367574.4:p.Glu376Ala
ENST00000378324.6:c.956A>C	ENSP00000367575.2:p.Glu319Ala
ENST00000403558.1:c.1241A>C	ENSP00000384420.1:p.Glu414Ala
ENST00000528996.1:c.313A>C	ENSP00000431226.1:n.313A>C
ENST00000530113.1:n.569A>C
ENST00000531133.5:c.613A>C	ENSP00000435431.1:n.613A>C
ENST00000531797.5:c.*137A>C	ENSP00000432554.1:n.*137A>C
ENST00000619430.1:c.349-106A>C	ENSP00000478572.1:n.349-106A>C
NM_000062.2:c.1112A>C , LRG_105t1:c.1112A>C	NP_000053.2:p.Glu371Ala
NM_001032295.1:c.1112A>C	NP_001027466.1:p.Glu371Ala
NM_000062.3:c.1112A>C MANE Select	NP_000053.2:p.Glu371Ala
NM_001032295.2:c.1112A>C	NP_001027466.1:p.Glu371Ala