Canonical Allele Identifier: CA6008285

Gene: SERPING1

Linked Data

• dbSNP Id: rs763451792
• ExAC: 11:57381936 T / C
• gnomAD v2: 11-57381936-T-C
• gnomAD v4: 11-57614463-T-C
• MyVariant Identifiers: chr11:g.57381936T>C (hg19) ; chr11:g.57614463T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614463T>C , CM000673.2:g.57614463T>C	GRCh38
NC_000011.9:g.57381936T>C , CM000673.1:g.57381936T>C	GRCh37
NC_000011.8:g.57138512T>C	NCBI36
NG_009625.1:g.21910T>C , LRG_105:g.21910T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1385T>C MANE Select	ENSP00000278407.4:p.Ile462Thr
ENST00000528996.2:c.*282T>C	ENSP00000431226.2:n.*282T>C
ENST00000531605.2:c.*1161T>C	ENSP00000503752.1:n.*1161T>C
ENST00000619430.2:c.1181T>C	ENSP00000478572.2:p.Ile394Thr
ENST00000676670.1:c.1385T>C	ENSP00000504807.1:p.Ile462Thr
ENST00000676741.1:n.2467T>C
ENST00000677624.1:c.*805T>C	ENSP00000503979.1:n.*805T>C
ENST00000677625.1:c.1331T>C	ENSP00000502857.1:p.Ile444Thr
ENST00000677856.1:n.1638T>C
ENST00000677915.1:c.*282T>C	ENSP00000503118.1:n.*282T>C
ENST00000678533.1:c.*939T>C	ENSP00000503873.1:n.*939T>C
ENST00000678592.1:c.*325T>C	ENSP00000504424.1:n.*325T>C
ENST00000278407.8:c.1385T>C	ENSP00000278407.4:p.Ile462Thr
ENST00000340687.10:c.1274T>C	ENSP00000341861.6:p.Ile425Thr
ENST00000378323.8:c.1400T>C	ENSP00000367574.4:p.Ile467Thr
ENST00000378324.6:c.1229T>C	ENSP00000367575.2:p.Ile410Thr
ENST00000403558.1:c.1514T>C	ENSP00000384420.1:p.Ile505Thr
ENST00000528996.1:c.586T>C	ENSP00000431226.1:n.586T>C
ENST00000530113.1:n.842T>C
ENST00000531133.5:c.886T>C	ENSP00000435431.1:n.886T>C
ENST00000531797.5:c.*410T>C	ENSP00000432554.1:n.*410T>C
ENST00000619430.1:c.516T>C	ENSP00000478572.1:n.516T>C
NM_000062.2:c.1385T>C , LRG_105t1:c.1385T>C	NP_000053.2:p.Ile462Thr
NM_001032295.1:c.1385T>C	NP_001027466.1:p.Ile462Thr
NM_000062.3:c.1385T>C MANE Select	NP_000053.2:p.Ile462Thr
NM_001032295.2:c.1385T>C	NP_001027466.1:p.Ile462Thr