Canonical Allele Identifier: CA380694912

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57600063-C-T
• MyVariant Identifiers: chr11:g.57367536C>T (hg19) ; chr11:g.57600063C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600063C>T , CM000673.2:g.57600063C>T	GRCh38
NC_000011.9:g.57367536C>T , CM000673.1:g.57367536C>T	GRCh37
NC_000011.8:g.57124112C>T	NCBI36
NG_009625.1:g.7510C>T , LRG_105:g.7510C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.236C>T MANE Select	ENSP00000278407.4:p.Thr79Ile
ENST00000528996.2:c.58+1735C>T	ENSP00000431226.2:n.58+1735C>T
ENST00000531605.2:c.51+1742C>T	ENSP00000503752.1:n.51+1742C>T
ENST00000619430.2:c.236C>T	ENSP00000478572.2:p.Thr79Ile
ENST00000676670.1:c.236C>T	ENSP00000504807.1:p.Thr79Ile
ENST00000676741.1:n.1318C>T
ENST00000677275.1:n.223C>T
ENST00000677624.1:c.236C>T	ENSP00000503979.1:p.Thr79Ile
ENST00000677625.1:c.236C>T	ENSP00000502857.1:p.Thr79Ile
ENST00000677856.1:n.295C>T
ENST00000677915.1:c.236C>T	ENSP00000503118.1:p.Thr79Ile
ENST00000678533.1:c.51+1742C>T	ENSP00000503873.1:n.51+1742C>T
ENST00000678592.1:c.236C>T	ENSP00000504424.1:p.Thr79Ile
ENST00000278407.8:c.236C>T	ENSP00000278407.4:p.Thr79Ile
ENST00000340687.10:c.236C>T	ENSP00000341861.6:p.Thr79Ile
ENST00000378323.8:c.251C>T	ENSP00000367574.4:p.Thr84Ile
ENST00000378324.6:c.80C>T	ENSP00000367575.2:p.Thr27Ile
ENST00000403558.1:c.338C>T	ENSP00000384420.1:p.Thr113Ile
ENST00000405496.5:c.236C>T	ENSP00000384561.1:p.Thr79Ile
ENST00000457869.1:c.338C>T	ENSP00000399746.1:p.Thr113Ile
ENST00000531133.5:c.51+1742C>T	ENSP00000435431.1:n.51+1742C>T
ENST00000531797.5:c.51+1742C>T	ENSP00000432554.1:n.51+1742C>T
ENST00000619430.1:c.236C>T	ENSP00000478572.1:p.Thr79Ile
NM_000062.2:c.236C>T , LRG_105t1:c.236C>T	NP_000053.2:p.Thr79Ile
NM_001032295.1:c.236C>T	NP_001027466.1:p.Thr79Ile
NM_000062.3:c.236C>T MANE Select	NP_000053.2:p.Thr79Ile
NM_001032295.2:c.236C>T	NP_001027466.1:p.Thr79Ile