Canonical Allele Identifier: CA474806718

Gene: SERPING1

Linked Data

• dbSNP Id: rs1945512855
• MyVariant Identifiers: chr11:g.57381838G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614365G>C , CM000673.2:g.57614365G>C	GRCh38
NC_000011.9:g.57381838G>C , CM000673.1:g.57381838G>C	GRCh37
NC_000011.8:g.57138414G>C	NCBI36
NG_009625.1:g.21812G>C , LRG_105:g.21812G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1287G>C MANE Select	ENSP00000278407.4:p.Gly429=
ENST00000528996.2:c.*184G>C	ENSP00000431226.2:n.*184G>C
ENST00000531605.2:c.*1063G>C	ENSP00000503752.1:n.*1063G>C
ENST00000619430.2:c.1083G>C	ENSP00000478572.2:p.Gly361=
ENST00000676670.1:c.1287G>C	ENSP00000504807.1:p.Gly429=
ENST00000676741.1:n.2369G>C
ENST00000677624.1:c.*707G>C	ENSP00000503979.1:n.*707G>C
ENST00000677625.1:c.1233G>C	ENSP00000502857.1:p.Gly411=
ENST00000677856.1:n.1540G>C
ENST00000677915.1:c.*184G>C	ENSP00000503118.1:n.*184G>C
ENST00000678533.1:c.*841G>C	ENSP00000503873.1:n.*841G>C
ENST00000678592.1:c.*227G>C	ENSP00000504424.1:n.*227G>C
ENST00000278407.8:c.1287G>C	ENSP00000278407.4:p.Gly429=
ENST00000340687.10:c.1176G>C	ENSP00000341861.6:p.Gly392=
ENST00000378323.8:c.1302G>C	ENSP00000367574.4:p.Gly434=
ENST00000378324.6:c.1131G>C	ENSP00000367575.2:p.Gly377=
ENST00000403558.1:c.1416G>C	ENSP00000384420.1:p.Gly472=
ENST00000528996.1:c.488G>C	ENSP00000431226.1:n.488G>C
ENST00000530113.1:n.744G>C
ENST00000531133.5:c.788G>C	ENSP00000435431.1:n.788G>C
ENST00000531797.5:c.*312G>C	ENSP00000432554.1:n.*312G>C
ENST00000619430.1:c.418G>C	ENSP00000478572.1:n.418G>C
NM_000062.2:c.1287G>C , LRG_105t1:c.1287G>C	NP_000053.2:p.Gly429=
NM_001032295.1:c.1287G>C	NP_001027466.1:p.Gly429=
NM_000062.3:c.1287G>C MANE Select	NP_000053.2:p.Gly429=
NM_001032295.2:c.1287G>C	NP_001027466.1:p.Gly429=