Canonical Allele Identifier: CA223024584

Gene: SERPING1

Linked Data

• dbSNP Id: rs1044921353
• gnomAD v3: 11-57614692-T-C
• gnomAD v4: 11-57614692-T-C
• MyVariant Identifiers: chr11:g.57382165T>C (hg19) ; chr11:g.57614692T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614692T>C , CM000673.2:g.57614692T>C	GRCh38
NC_000011.9:g.57382165T>C , CM000673.1:g.57382165T>C	GRCh37
NC_000011.8:g.57138741T>C	NCBI36
NG_009625.1:g.22139T>C , LRG_105:g.22139T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*111T>C MANE Select	ENSP00000278407.4:n.*111T>C
ENST00000528996.2:c.*511T>C	ENSP00000431226.2:n.*511T>C
ENST00000531605.2:c.*1390T>C	ENSP00000503752.1:n.*1390T>C
ENST00000619430.2:c.*111T>C	ENSP00000478572.2:n.*111T>C
ENST00000676670.1:c.*15+96T>C	ENSP00000504807.1:n.*15+96T>C
ENST00000676741.1:n.2696T>C
ENST00000677624.1:c.*1034T>C	ENSP00000503979.1:n.*1034T>C
ENST00000677625.1:c.*111T>C	ENSP00000502857.1:n.*111T>C
ENST00000677856.1:n.1867T>C
ENST00000677915.1:c.*511T>C	ENSP00000503118.1:n.*511T>C
ENST00000678533.1:c.*1072+96T>C	ENSP00000503873.1:n.*1072+96T>C
ENST00000678592.1:c.*554T>C	ENSP00000504424.1:n.*554T>C
ENST00000278407.8:c.*111T>C	ENSP00000278407.4:n.*111T>C
ENST00000340687.10:c.*111T>C	ENSP00000341861.6:n.*111T>C
ENST00000378323.8:c.*111T>C	ENSP00000367574.4:n.*111T>C
ENST00000378324.6:c.*111T>C	ENSP00000367575.2:n.*111T>C
ENST00000403558.1:c.*111T>C	ENSP00000384420.1:n.*111T>C
ENST00000528996.1:c.815T>C	ENSP00000431226.1:n.815T>C
ENST00000531797.5:c.*639T>C	ENSP00000432554.1:n.*639T>C
NM_000062.2:c.*111T>C , LRG_105t1:c.*111T>C	NP_000053.2:n.*111T>C
NM_001032295.1:c.*111T>C	NP_001027466.1:n.*111T>C
NM_000062.3:c.*111T>C MANE Select	NP_000053.2:n.*111T>C
NM_001032295.2:c.*111T>C	NP_001027466.1:n.*111T>C