Canonical Allele Identifier: CA380690327

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381842A>C (hg19) ; chr11:g.57614369A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614369A>C , CM000673.2:g.57614369A>C	GRCh38
NC_000011.9:g.57381842A>C , CM000673.1:g.57381842A>C	GRCh37
NC_000011.8:g.57138418A>C	NCBI36
NG_009625.1:g.21816A>C , LRG_105:g.21816A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1291A>C MANE Select	ENSP00000278407.4:p.Thr431Pro
ENST00000528996.2:c.*188A>C	ENSP00000431226.2:n.*188A>C
ENST00000531605.2:c.*1067A>C	ENSP00000503752.1:n.*1067A>C
ENST00000619430.2:c.1087A>C	ENSP00000478572.2:p.Thr363Pro
ENST00000676670.1:c.1291A>C	ENSP00000504807.1:p.Thr431Pro
ENST00000676741.1:n.2373A>C
ENST00000677624.1:c.*711A>C	ENSP00000503979.1:n.*711A>C
ENST00000677625.1:c.1237A>C	ENSP00000502857.1:p.Thr413Pro
ENST00000677856.1:n.1544A>C
ENST00000677915.1:c.*188A>C	ENSP00000503118.1:n.*188A>C
ENST00000678533.1:c.*845A>C	ENSP00000503873.1:n.*845A>C
ENST00000678592.1:c.*231A>C	ENSP00000504424.1:n.*231A>C
ENST00000278407.8:c.1291A>C	ENSP00000278407.4:p.Thr431Pro
ENST00000340687.10:c.1180A>C	ENSP00000341861.6:p.Thr394Pro
ENST00000378323.8:c.1306A>C	ENSP00000367574.4:p.Thr436Pro
ENST00000378324.6:c.1135A>C	ENSP00000367575.2:p.Thr379Pro
ENST00000403558.1:c.1420A>C	ENSP00000384420.1:p.Thr474Pro
ENST00000528996.1:c.492A>C	ENSP00000431226.1:n.492A>C
ENST00000530113.1:n.748A>C
ENST00000531133.5:c.792A>C	ENSP00000435431.1:n.792A>C
ENST00000531797.5:c.*316A>C	ENSP00000432554.1:n.*316A>C
ENST00000619430.1:c.422A>C	ENSP00000478572.1:n.422A>C
NM_000062.2:c.1291A>C , LRG_105t1:c.1291A>C	NP_000053.2:p.Thr431Pro
NM_001032295.1:c.1291A>C	NP_001027466.1:p.Thr431Pro
NM_000062.3:c.1291A>C MANE Select	NP_000053.2:p.Thr431Pro
NM_001032295.2:c.1291A>C	NP_001027466.1:p.Thr431Pro