Canonical Allele Identifier: CA599664866

Gene: SERPING1

Linked Data

• gnomAD v2: 11-57378408-C-CTT
• gnomAD v3: 11-57610935-C-CTT
• gnomAD v4: 11-57610935-C-CTT
• MyVariant Identifiers: chr11:g.57378409_57378410insTT (hg19) ; chr11:g.57610936_57610937insTT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57610944_57610945dup , CM000673.2:g.57610944_57610945dup	GRCh38
NC_000011.9:g.57378417_57378418dup , CM000673.1:g.57378417_57378418dup	GRCh37
NC_000011.8:g.57134993_57134994dup	NCBI36
NG_009625.1:g.18391_18392dup , LRG_105:g.18391_18392dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1030-773_1030-772dup MANE Select	ENSP00000278407.4:n.1030-773_1030-772dup
ENST00000528996.2:c.59-782_59-781dup	ENSP00000431226.2:n.59-782_59-781dup
ENST00000531605.2:c.*806-773_*806-772dup	ENSP00000503752.1:n.*806-773_*806-772dup
ENST00000619430.2:c.826-773_826-772dup	ENSP00000478572.2:n.826-773_826-772dup
ENST00000676670.1:c.1030-773_1030-772dup	ENSP00000504807.1:n.1030-773_1030-772dup
ENST00000676741.1:n.2112-773_2112-772dup
ENST00000677624.1:c.*450-773_*450-772dup	ENSP00000503979.1:n.*450-773_*450-772dup
ENST00000677625.1:c.1030-827_1030-826dup	ENSP00000502857.1:n.1030-827_1030-826dup
ENST00000677856.1:n.1283-773_1283-772dup
ENST00000677915.1:c.686-773_686-772dup	ENSP00000503118.1:n.686-773_686-772dup
ENST00000678533.1:c.*584-773_*584-772dup	ENSP00000503873.1:n.*584-773_*584-772dup
ENST00000678592.1:c.1119-773_1119-772dup	ENSP00000504424.1:n.1119-773_1119-772dup
ENST00000278407.8:c.1030-773_1030-772dup	ENSP00000278407.4:n.1030-773_1030-772dup
ENST00000340687.10:c.1030-884_1030-883dup	ENSP00000341861.6:n.1030-884_1030-883dup
ENST00000378323.8:c.1045-773_1045-772dup	ENSP00000367574.4:n.1045-773_1045-772dup
ENST00000378324.6:c.874-773_874-772dup	ENSP00000367575.2:n.874-773_874-772dup
ENST00000403558.1:c.1159-773_1159-772dup	ENSP00000384420.1:n.1159-773_1159-772dup
ENST00000528996.1:c.231-773_231-772dup	ENSP00000431226.1:n.231-773_231-772dup
ENST00000531133.5:c.531-773_531-772dup	ENSP00000435431.1:n.531-773_531-772dup
ENST00000531797.5:c.*55-773_*55-772dup	ENSP00000432554.1:n.*55-773_*55-772dup
ENST00000619430.1:c.349-961_349-960dup	ENSP00000478572.1:n.349-961_349-960dup
NM_000062.2:c.1030-773_1030-772dup , LRG_105t1:c.1030-773_1030-772dup	NP_000053.2:n.1030-773_1030-772dup
NM_001032295.1:c.1030-773_1030-772dup	NP_001027466.1:n.1030-773_1030-772dup
NM_000062.3:c.1030-773_1030-772dup MANE Select	NP_000053.2:n.1030-773_1030-772dup
NM_001032295.2:c.1030-773_1030-772dup	NP_001027466.1:n.1030-773_1030-772dup