Canonical Allele Identifier: CA380690347

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381847G>C (hg19) ; chr11:g.57614374G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614374G>C , CM000673.2:g.57614374G>C	GRCh38
NC_000011.9:g.57381847G>C , CM000673.1:g.57381847G>C	GRCh37
NC_000011.8:g.57138423G>C	NCBI36
NG_009625.1:g.21821G>C , LRG_105:g.21821G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1296G>C MANE Select	ENSP00000278407.4:p.Glu432Asp
ENST00000528996.2:c.*193G>C	ENSP00000431226.2:n.*193G>C
ENST00000531605.2:c.*1072G>C	ENSP00000503752.1:n.*1072G>C
ENST00000619430.2:c.1092G>C	ENSP00000478572.2:p.Glu364Asp
ENST00000676670.1:c.1296G>C	ENSP00000504807.1:p.Glu432Asp
ENST00000676741.1:n.2378G>C
ENST00000677624.1:c.*716G>C	ENSP00000503979.1:n.*716G>C
ENST00000677625.1:c.1242G>C	ENSP00000502857.1:p.Glu414Asp
ENST00000677856.1:n.1549G>C
ENST00000677915.1:c.*193G>C	ENSP00000503118.1:n.*193G>C
ENST00000678533.1:c.*850G>C	ENSP00000503873.1:n.*850G>C
ENST00000678592.1:c.*236G>C	ENSP00000504424.1:n.*236G>C
ENST00000278407.8:c.1296G>C	ENSP00000278407.4:p.Glu432Asp
ENST00000340687.10:c.1185G>C	ENSP00000341861.6:p.Glu395Asp
ENST00000378323.8:c.1311G>C	ENSP00000367574.4:p.Glu437Asp
ENST00000378324.6:c.1140G>C	ENSP00000367575.2:p.Glu380Asp
ENST00000403558.1:c.1425G>C	ENSP00000384420.1:p.Glu475Asp
ENST00000528996.1:c.497G>C	ENSP00000431226.1:n.497G>C
ENST00000530113.1:n.753G>C
ENST00000531133.5:c.797G>C	ENSP00000435431.1:n.797G>C
ENST00000531797.5:c.*321G>C	ENSP00000432554.1:n.*321G>C
ENST00000619430.1:c.427G>C	ENSP00000478572.1:n.427G>C
NM_000062.2:c.1296G>C , LRG_105t1:c.1296G>C	NP_000053.2:p.Glu432Asp
NM_001032295.1:c.1296G>C	NP_001027466.1:p.Glu432Asp
NM_000062.3:c.1296G>C MANE Select	NP_000053.2:p.Glu432Asp
NM_001032295.2:c.1296G>C	NP_001027466.1:p.Glu432Asp