Canonical Allele Identifier: CA380695521
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57600320A>T , CM000673.2:g.57600320A>T GRCh38
NC_000011.9:g.57367793A>T , CM000673.1:g.57367793A>T GRCh37
NC_000011.8:g.57124369A>T NCBI36
NG_009625.1:g.7767A>T , LRG_105:g.7767A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.493A>T MANE Select ENSP00000278407.4:p.Thr165Ser
ENST00000528996.2:c.58+1992A>T ENSP00000431226.2:n.58+1992A>T
ENST00000531605.2:c.52-1715A>T ENSP00000503752.1:n.52-1715A>T
ENST00000619430.2:c.493A>T ENSP00000478572.2:p.Thr165Ser
ENST00000676670.1:c.493A>T ENSP00000504807.1:p.Thr165Ser
ENST00000676741.1:n.1575A>T
ENST00000677275.1:n.480A>T
ENST00000677624.1:c.493A>T ENSP00000503979.1:p.Thr165Ser
ENST00000677625.1:c.493A>T ENSP00000502857.1:p.Thr165Ser
ENST00000677856.1:n.552A>T
ENST00000677915.1:c.493A>T ENSP00000503118.1:p.Thr165Ser
ENST00000678533.1:c.52-1715A>T ENSP00000503873.1:n.52-1715A>T
ENST00000678592.1:c.493A>T ENSP00000504424.1:p.Thr165Ser
ENST00000278407.8:c.493A>T ENSP00000278407.4:p.Thr165Ser
ENST00000340687.10:c.493A>T ENSP00000341861.6:p.Thr165Ser
ENST00000378323.8:c.508A>T ENSP00000367574.4:p.Thr170Ser
ENST00000378324.6:c.337A>T ENSP00000367575.2:p.Thr113Ser
ENST00000403558.1:c.595A>T ENSP00000384420.1:p.Thr199Ser
ENST00000531133.5:c.52-1715A>T ENSP00000435431.1:n.52-1715A>T
ENST00000531797.5:c.52-1715A>T ENSP00000432554.1:n.52-1715A>T
ENST00000619430.1:c.348+145A>T ENSP00000478572.1:n.348+145A>T
NM_000062.2:c.493A>T , LRG_105t1:c.493A>T NP_000053.2:p.Thr165Ser
NM_001032295.1:c.493A>T NP_001027466.1:p.Thr165Ser
NM_000062.3:c.493A>T MANE Select NP_000053.2:p.Thr165Ser
NM_001032295.2:c.493A>T NP_001027466.1:p.Thr165Ser