Canonical Allele Identifier: CA380690345

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381846A>C (hg19) ; chr11:g.57614373A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614373A>C , CM000673.2:g.57614373A>C	GRCh38
NC_000011.9:g.57381846A>C , CM000673.1:g.57381846A>C	GRCh37
NC_000011.8:g.57138422A>C	NCBI36
NG_009625.1:g.21820A>C , LRG_105:g.21820A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1295A>C MANE Select	ENSP00000278407.4:p.Glu432Ala
ENST00000528996.2:c.*192A>C	ENSP00000431226.2:n.*192A>C
ENST00000531605.2:c.*1071A>C	ENSP00000503752.1:n.*1071A>C
ENST00000619430.2:c.1091A>C	ENSP00000478572.2:p.Glu364Ala
ENST00000676670.1:c.1295A>C	ENSP00000504807.1:p.Glu432Ala
ENST00000676741.1:n.2377A>C
ENST00000677624.1:c.*715A>C	ENSP00000503979.1:n.*715A>C
ENST00000677625.1:c.1241A>C	ENSP00000502857.1:p.Glu414Ala
ENST00000677856.1:n.1548A>C
ENST00000677915.1:c.*192A>C	ENSP00000503118.1:n.*192A>C
ENST00000678533.1:c.*849A>C	ENSP00000503873.1:n.*849A>C
ENST00000678592.1:c.*235A>C	ENSP00000504424.1:n.*235A>C
ENST00000278407.8:c.1295A>C	ENSP00000278407.4:p.Glu432Ala
ENST00000340687.10:c.1184A>C	ENSP00000341861.6:p.Glu395Ala
ENST00000378323.8:c.1310A>C	ENSP00000367574.4:p.Glu437Ala
ENST00000378324.6:c.1139A>C	ENSP00000367575.2:p.Glu380Ala
ENST00000403558.1:c.1424A>C	ENSP00000384420.1:p.Glu475Ala
ENST00000528996.1:c.496A>C	ENSP00000431226.1:n.496A>C
ENST00000530113.1:n.752A>C
ENST00000531133.5:c.796A>C	ENSP00000435431.1:n.796A>C
ENST00000531797.5:c.*320A>C	ENSP00000432554.1:n.*320A>C
ENST00000619430.1:c.426A>C	ENSP00000478572.1:n.426A>C
NM_000062.2:c.1295A>C , LRG_105t1:c.1295A>C	NP_000053.2:p.Glu432Ala
NM_001032295.1:c.1295A>C	NP_001027466.1:p.Glu432Ala
NM_000062.3:c.1295A>C MANE Select	NP_000053.2:p.Glu432Ala
NM_001032295.2:c.1295A>C	NP_001027466.1:p.Glu432Ala