Canonical Allele Identifier: CA380694857

Gene: SERPING1

Linked Data

• ClinVar Variation Id: 1074911
• ClinVar RCV Id: RCV001388357
• dbSNP Id: rs2135308212
• MyVariant Identifiers: chr11:g.57367521C>A (hg19) ; chr11:g.57600048C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600048C>A , CM000673.2:g.57600048C>A	GRCh38
NC_000011.9:g.57367521C>A , CM000673.1:g.57367521C>A	GRCh37
NC_000011.8:g.57124097C>A	NCBI36
NG_009625.1:g.7495C>A , LRG_105:g.7495C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.221C>A MANE Select	ENSP00000278407.4:p.Ser74Ter
ENST00000528996.2:c.58+1720C>A	ENSP00000431226.2:n.58+1720C>A
ENST00000531605.2:c.51+1727C>A	ENSP00000503752.1:n.51+1727C>A
ENST00000619430.2:c.221C>A	ENSP00000478572.2:p.Ser74Ter
ENST00000676670.1:c.221C>A	ENSP00000504807.1:p.Ser74Ter
ENST00000676741.1:n.1303C>A
ENST00000677275.1:n.208C>A
ENST00000677624.1:c.221C>A	ENSP00000503979.1:p.Ser74Ter
ENST00000677625.1:c.221C>A	ENSP00000502857.1:p.Ser74Ter
ENST00000677856.1:n.280C>A
ENST00000677915.1:c.221C>A	ENSP00000503118.1:p.Ser74Ter
ENST00000678533.1:c.51+1727C>A	ENSP00000503873.1:n.51+1727C>A
ENST00000678592.1:c.221C>A	ENSP00000504424.1:p.Ser74Ter
ENST00000278407.8:c.221C>A	ENSP00000278407.4:p.Ser74Ter
ENST00000340687.10:c.221C>A	ENSP00000341861.6:p.Ser74Ter
ENST00000378323.8:c.236C>A	ENSP00000367574.4:p.Ser79Ter
ENST00000378324.6:c.65C>A	ENSP00000367575.2:p.Ser22Ter
ENST00000403558.1:c.323C>A	ENSP00000384420.1:p.Ser108Ter
ENST00000405496.5:c.221C>A	ENSP00000384561.1:p.Ser74Ter
ENST00000457869.1:c.323C>A	ENSP00000399746.1:p.Ser108Ter
ENST00000531133.5:c.51+1727C>A	ENSP00000435431.1:n.51+1727C>A
ENST00000531797.5:c.51+1727C>A	ENSP00000432554.1:n.51+1727C>A
ENST00000619430.1:c.221C>A	ENSP00000478572.1:p.Ser74Ter
NM_000062.2:c.221C>A , LRG_105t1:c.221C>A	NP_000053.2:p.Ser74Ter
NM_001032295.1:c.221C>A	NP_001027466.1:p.Ser74Ter
NM_000062.3:c.221C>A MANE Select	NP_000053.2:p.Ser74Ter
NM_001032295.2:c.221C>A	NP_001027466.1:p.Ser74Ter