Canonical Allele Identifier: CA380702509

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57611759-C-G
• MyVariant Identifiers: chr11:g.57379232C>G (hg19) ; chr11:g.57611759C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611759C>G , CM000673.2:g.57611759C>G	GRCh38
NC_000011.9:g.57379232C>G , CM000673.1:g.57379232C>G	GRCh37
NC_000011.8:g.57135808C>G	NCBI36
NG_009625.1:g.19206C>G , LRG_105:g.19206C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1072C>G MANE Select	ENSP00000278407.4:p.Leu358Val
ENST00000528996.2:c.92C>G	ENSP00000431226.2:p.Pro31Arg
ENST00000531605.2:c.*848C>G	ENSP00000503752.1:n.*848C>G
ENST00000619430.2:c.868C>G	ENSP00000478572.2:p.Leu290Val
ENST00000676670.1:c.1072C>G	ENSP00000504807.1:p.Leu358Val
ENST00000676741.1:n.2154C>G
ENST00000677624.1:c.*492C>G	ENSP00000503979.1:n.*492C>G
ENST00000677625.1:c.1030-12C>G	ENSP00000502857.1:n.1030-12C>G
ENST00000677856.1:n.1325C>G
ENST00000677915.1:c.728C>G	ENSP00000503118.1:p.Pro243Arg
ENST00000678533.1:c.*626C>G	ENSP00000503873.1:n.*626C>G
ENST00000678592.1:c.*12C>G	ENSP00000504424.1:n.*12C>G
ENST00000278407.8:c.1072C>G	ENSP00000278407.4:p.Leu358Val
ENST00000340687.10:c.1030-69C>G	ENSP00000341861.6:n.1030-69C>G
ENST00000378323.8:c.1087C>G	ENSP00000367574.4:p.Leu363Val
ENST00000378324.6:c.916C>G	ENSP00000367575.2:p.Leu306Val
ENST00000403558.1:c.1201C>G	ENSP00000384420.1:p.Leu401Val
ENST00000528996.1:c.273C>G	ENSP00000431226.1:n.273C>G
ENST00000530113.1:n.529C>G
ENST00000531133.5:c.573C>G	ENSP00000435431.1:n.573C>G
ENST00000531797.5:c.*97C>G	ENSP00000432554.1:n.*97C>G
ENST00000619430.1:c.349-146C>G	ENSP00000478572.1:n.349-146C>G
NM_000062.2:c.1072C>G , LRG_105t1:c.1072C>G	NP_000053.2:p.Leu358Val
NM_001032295.1:c.1072C>G	NP_001027466.1:p.Leu358Val
NM_000062.3:c.1072C>G MANE Select	NP_000053.2:p.Leu358Val
NM_001032295.2:c.1072C>G	NP_001027466.1:p.Leu358Val