Canonical Allele Identifier: CA223054092

Gene: SERPING1

Linked Data

• dbSNP Id: rs888195036
• MyVariant Identifiers: chr11:g.57367575C>T (hg19) ; chr11:g.57600102C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600102C>T , CM000673.2:g.57600102C>T	GRCh38
NC_000011.9:g.57367575C>T , CM000673.1:g.57367575C>T	GRCh37
NC_000011.8:g.57124151C>T	NCBI36
NG_009625.1:g.7549C>T , LRG_105:g.7549C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.275C>T MANE Select	ENSP00000278407.4:p.Thr92Ile
ENST00000528996.2:c.58+1774C>T	ENSP00000431226.2:n.58+1774C>T
ENST00000531605.2:c.51+1781C>T	ENSP00000503752.1:n.51+1781C>T
ENST00000619430.2:c.275C>T	ENSP00000478572.2:p.Thr92Ile
ENST00000676670.1:c.275C>T	ENSP00000504807.1:p.Thr92Ile
ENST00000676741.1:n.1357C>T
ENST00000677275.1:n.262C>T
ENST00000677624.1:c.275C>T	ENSP00000503979.1:p.Thr92Ile
ENST00000677625.1:c.275C>T	ENSP00000502857.1:p.Thr92Ile
ENST00000677856.1:n.334C>T
ENST00000677915.1:c.275C>T	ENSP00000503118.1:p.Thr92Ile
ENST00000678533.1:c.51+1781C>T	ENSP00000503873.1:n.51+1781C>T
ENST00000678592.1:c.275C>T	ENSP00000504424.1:p.Thr92Ile
ENST00000278407.8:c.275C>T	ENSP00000278407.4:p.Thr92Ile
ENST00000340687.10:c.275C>T	ENSP00000341861.6:p.Thr92Ile
ENST00000378323.8:c.290C>T	ENSP00000367574.4:p.Thr97Ile
ENST00000378324.6:c.119C>T	ENSP00000367575.2:p.Thr40Ile
ENST00000403558.1:c.377C>T	ENSP00000384420.1:p.Thr126Ile
ENST00000405496.5:c.275C>T	ENSP00000384561.1:p.Thr92Ile
ENST00000531133.5:c.51+1781C>T	ENSP00000435431.1:n.51+1781C>T
ENST00000531797.5:c.51+1781C>T	ENSP00000432554.1:n.51+1781C>T
ENST00000619430.1:c.275C>T	ENSP00000478572.1:p.Thr92Ile
NM_000062.2:c.275C>T , LRG_105t1:c.275C>T	NP_000053.2:p.Thr92Ile
NM_001032295.1:c.275C>T	NP_001027466.1:p.Thr92Ile
NM_000062.3:c.275C>T MANE Select	NP_000053.2:p.Thr92Ile
NM_001032295.2:c.275C>T	NP_001027466.1:p.Thr92Ile