Canonical Allele Identifier: CA380690773

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381965G>C (hg19) ; chr11:g.57614492G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614492G>C , CM000673.2:g.57614492G>C	GRCh38
NC_000011.9:g.57381965G>C , CM000673.1:g.57381965G>C	GRCh37
NC_000011.8:g.57138541G>C	NCBI36
NG_009625.1:g.21939G>C , LRG_105:g.21939G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1414G>C MANE Select	ENSP00000278407.4:p.Glu472Gln
ENST00000528996.2:c.*311G>C	ENSP00000431226.2:n.*311G>C
ENST00000531605.2:c.*1190G>C	ENSP00000503752.1:n.*1190G>C
ENST00000619430.2:c.1210G>C	ENSP00000478572.2:p.Glu404Gln
ENST00000676670.1:c.1414G>C	ENSP00000504807.1:p.Glu472Gln
ENST00000676741.1:n.2496G>C
ENST00000677624.1:c.*834G>C	ENSP00000503979.1:n.*834G>C
ENST00000677625.1:c.1360G>C	ENSP00000502857.1:p.Glu454Gln
ENST00000677856.1:n.1667G>C
ENST00000677915.1:c.*311G>C	ENSP00000503118.1:n.*311G>C
ENST00000678533.1:c.*968G>C	ENSP00000503873.1:n.*968G>C
ENST00000678592.1:c.*354G>C	ENSP00000504424.1:n.*354G>C
ENST00000278407.8:c.1414G>C	ENSP00000278407.4:p.Glu472Gln
ENST00000340687.10:c.1303G>C	ENSP00000341861.6:p.Glu435Gln
ENST00000378323.8:c.1429G>C	ENSP00000367574.4:p.Glu477Gln
ENST00000378324.6:c.1258G>C	ENSP00000367575.2:p.Glu420Gln
ENST00000403558.1:c.1543G>C	ENSP00000384420.1:p.Glu515Gln
ENST00000528996.1:c.615G>C	ENSP00000431226.1:n.615G>C
ENST00000530113.1:n.871G>C
ENST00000531133.5:c.915G>C	ENSP00000435431.1:n.915G>C
ENST00000531797.5:c.*439G>C	ENSP00000432554.1:n.*439G>C
ENST00000619430.1:c.545G>C	ENSP00000478572.1:n.545G>C
NM_000062.2:c.1414G>C , LRG_105t1:c.1414G>C	NP_000053.2:p.Glu472Gln
NM_001032295.1:c.1414G>C	NP_001027466.1:p.Glu472Gln
NM_000062.3:c.1414G>C MANE Select	NP_000053.2:p.Glu472Gln
NM_001032295.2:c.1414G>C	NP_001027466.1:p.Glu472Gln