Canonical Allele Identifier: CA223056775

Gene: SERPING1

Linked Data

• dbSNP Id: rs545919863
• MyVariant Identifiers: chr11:g.57378252T>G (hg19) ; chr11:g.57610779T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57610779T>G , CM000673.2:g.57610779T>G	GRCh38
NC_000011.9:g.57378252T>G , CM000673.1:g.57378252T>G	GRCh37
NC_000011.8:g.57134828T>G	NCBI36
NG_009625.1:g.18226T>G , LRG_105:g.18226T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1030-938T>G MANE Select	ENSP00000278407.4:n.1030-938T>G
ENST00000528996.2:c.59-947T>G	ENSP00000431226.2:n.59-947T>G
ENST00000531605.2:c.*806-938T>G	ENSP00000503752.1:n.*806-938T>G
ENST00000619430.2:c.826-938T>G	ENSP00000478572.2:n.826-938T>G
ENST00000676670.1:c.1030-938T>G	ENSP00000504807.1:n.1030-938T>G
ENST00000676741.1:n.2112-938T>G
ENST00000677624.1:c.*450-938T>G	ENSP00000503979.1:n.*450-938T>G
ENST00000677625.1:c.1030-992T>G	ENSP00000502857.1:n.1030-992T>G
ENST00000677856.1:n.1283-938T>G
ENST00000677915.1:c.686-938T>G	ENSP00000503118.1:n.686-938T>G
ENST00000678533.1:c.*584-938T>G	ENSP00000503873.1:n.*584-938T>G
ENST00000678592.1:c.1119-938T>G	ENSP00000504424.1:n.1119-938T>G
ENST00000278407.8:c.1030-938T>G	ENSP00000278407.4:n.1030-938T>G
ENST00000340687.10:c.1030-1049T>G	ENSP00000341861.6:n.1030-1049T>G
ENST00000378323.8:c.1045-938T>G	ENSP00000367574.4:n.1045-938T>G
ENST00000378324.6:c.874-938T>G	ENSP00000367575.2:n.874-938T>G
ENST00000403558.1:c.1159-938T>G	ENSP00000384420.1:n.1159-938T>G
ENST00000528996.1:c.231-938T>G	ENSP00000431226.1:n.231-938T>G
ENST00000531133.5:c.531-938T>G	ENSP00000435431.1:n.531-938T>G
ENST00000531797.5:c.*55-938T>G	ENSP00000432554.1:n.*55-938T>G
ENST00000619430.1:c.349-1126T>G	ENSP00000478572.1:n.349-1126T>G
NM_000062.2:c.1030-938T>G , LRG_105t1:c.1030-938T>G	NP_000053.2:n.1030-938T>G
NM_001032295.1:c.1030-938T>G	NP_001027466.1:n.1030-938T>G
NM_000062.3:c.1030-938T>G MANE Select	NP_000053.2:n.1030-938T>G
NM_001032295.2:c.1030-938T>G	NP_001027466.1:n.1030-938T>G