Canonical Allele Identifier: CA380690674

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381914G>C (hg19) ; chr11:g.57614441G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614441G>C , CM000673.2:g.57614441G>C	GRCh38
NC_000011.9:g.57381914G>C , CM000673.1:g.57381914G>C	GRCh37
NC_000011.8:g.57138490G>C	NCBI36
NG_009625.1:g.21888G>C , LRG_105:g.21888G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1363G>C MANE Select	ENSP00000278407.4:p.Glu455Gln
ENST00000528996.2:c.*260G>C	ENSP00000431226.2:n.*260G>C
ENST00000531605.2:c.*1139G>C	ENSP00000503752.1:n.*1139G>C
ENST00000619430.2:c.1159G>C	ENSP00000478572.2:p.Glu387Gln
ENST00000676670.1:c.1363G>C	ENSP00000504807.1:p.Glu455Gln
ENST00000676741.1:n.2445G>C
ENST00000677624.1:c.*783G>C	ENSP00000503979.1:n.*783G>C
ENST00000677625.1:c.1309G>C	ENSP00000502857.1:p.Glu437Gln
ENST00000677856.1:n.1616G>C
ENST00000677915.1:c.*260G>C	ENSP00000503118.1:n.*260G>C
ENST00000678533.1:c.*917G>C	ENSP00000503873.1:n.*917G>C
ENST00000678592.1:c.*303G>C	ENSP00000504424.1:n.*303G>C
ENST00000278407.8:c.1363G>C	ENSP00000278407.4:p.Glu455Gln
ENST00000340687.10:c.1252G>C	ENSP00000341861.6:p.Glu418Gln
ENST00000378323.8:c.1378G>C	ENSP00000367574.4:p.Glu460Gln
ENST00000378324.6:c.1207G>C	ENSP00000367575.2:p.Glu403Gln
ENST00000403558.1:c.1492G>C	ENSP00000384420.1:p.Glu498Gln
ENST00000528996.1:c.564G>C	ENSP00000431226.1:n.564G>C
ENST00000530113.1:n.820G>C
ENST00000531133.5:c.864G>C	ENSP00000435431.1:n.864G>C
ENST00000531797.5:c.*388G>C	ENSP00000432554.1:n.*388G>C
ENST00000619430.1:c.494G>C	ENSP00000478572.1:n.494G>C
NM_000062.2:c.1363G>C , LRG_105t1:c.1363G>C	NP_000053.2:p.Glu455Gln
NM_001032295.1:c.1363G>C	NP_001027466.1:p.Glu455Gln
NM_000062.3:c.1363G>C MANE Select	NP_000053.2:p.Glu455Gln
NM_001032295.2:c.1363G>C	NP_001027466.1:p.Glu455Gln