Canonical Allele Identifier: CA380699535

Gene: SERPING1

Linked Data

• dbSNP Id: rs1178615272
• gnomAD v3: 11-57606160-A-C
• gnomAD v4: 11-57606160-A-C
• MyVariant Identifiers: chr11:g.57373633A>C (hg19) ; chr11:g.57606160A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606160A>C , CM000673.2:g.57606160A>C	GRCh38
NC_000011.9:g.57373633A>C , CM000673.1:g.57373633A>C	GRCh37
NC_000011.8:g.57130209A>C	NCBI36
NG_009625.1:g.13607A>C , LRG_105:g.13607A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.836A>C MANE Select	ENSP00000278407.4:p.Asp279Ala
ENST00000528996.2:c.59-5566A>C	ENSP00000431226.2:n.59-5566A>C
ENST00000531605.2:c.*612A>C	ENSP00000503752.1:n.*612A>C
ENST00000619430.2:c.686-248A>C	ENSP00000478572.2:n.686-248A>C
ENST00000676670.1:c.836A>C	ENSP00000504807.1:p.Asp279Ala
ENST00000676741.1:n.1918A>C
ENST00000677624.1:c.*256A>C	ENSP00000503979.1:n.*256A>C
ENST00000677625.1:c.836A>C	ENSP00000502857.1:p.Asp279Ala
ENST00000677856.1:n.895A>C
ENST00000677915.1:c.685+3991A>C	ENSP00000503118.1:n.685+3991A>C
ENST00000678533.1:c.*390A>C	ENSP00000503873.1:n.*390A>C
ENST00000678592.1:c.836A>C	ENSP00000504424.1:p.Asp279Ala
ENST00000278407.8:c.836A>C	ENSP00000278407.4:p.Asp279Ala
ENST00000340687.10:c.836A>C	ENSP00000341861.6:p.Asp279Ala
ENST00000378323.8:c.851A>C	ENSP00000367574.4:p.Asp284Ala
ENST00000378324.6:c.680A>C	ENSP00000367575.2:p.Asp227Ala
ENST00000403558.1:c.938A>C	ENSP00000384420.1:p.Asp313Ala
ENST00000531133.5:c.337A>C	ENSP00000435431.1:n.337A>C
ENST00000531797.5:c.*54+3991A>C	ENSP00000432554.1:n.*54+3991A>C
ENST00000619430.1:c.349-5745A>C	ENSP00000478572.1:n.349-5745A>C
NM_000062.2:c.836A>C , LRG_105t1:c.836A>C	NP_000053.2:p.Asp279Ala
NM_001032295.1:c.836A>C	NP_001027466.1:p.Asp279Ala
NM_000062.3:c.836A>C MANE Select	NP_000053.2:p.Asp279Ala
NM_001032295.2:c.836A>C	NP_001027466.1:p.Asp279Ala