Canonical Allele Identifier: CA380698831
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606061G>T , CM000673.2:g.57606061G>T GRCh38
NC_000011.9:g.57373534G>T , CM000673.1:g.57373534G>T GRCh37
NC_000011.8:g.57130110G>T NCBI36
NG_009625.1:g.13508G>T , LRG_105:g.13508G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.737G>T MANE Select ENSP00000278407.4:p.Ser246Ile
ENST00000528996.2:c.59-5665G>T ENSP00000431226.2:n.59-5665G>T
ENST00000531605.2:c.*513G>T ENSP00000503752.1:n.*513G>T
ENST00000619430.2:c.686-347G>T ENSP00000478572.2:n.686-347G>T
ENST00000676670.1:c.737G>T ENSP00000504807.1:p.Ser246Ile
ENST00000676741.1:n.1819G>T
ENST00000677624.1:c.*157G>T ENSP00000503979.1:n.*157G>T
ENST00000677625.1:c.737G>T ENSP00000502857.1:p.Ser246Ile
ENST00000677856.1:n.796G>T
ENST00000677915.1:c.685+3892G>T ENSP00000503118.1:n.685+3892G>T
ENST00000678533.1:c.*291G>T ENSP00000503873.1:n.*291G>T
ENST00000678592.1:c.737G>T ENSP00000504424.1:p.Ser246Ile
ENST00000278407.8:c.737G>T ENSP00000278407.4:p.Ser246Ile
ENST00000340687.10:c.737G>T ENSP00000341861.6:p.Ser246Ile
ENST00000378323.8:c.752G>T ENSP00000367574.4:p.Ser251Ile
ENST00000378324.6:c.581G>T ENSP00000367575.2:p.Ser194Ile
ENST00000403558.1:c.839G>T ENSP00000384420.1:p.Ser280Ile
ENST00000531133.5:c.238G>T ENSP00000435431.1:n.238G>T
ENST00000531797.5:c.*54+3892G>T ENSP00000432554.1:n.*54+3892G>T
ENST00000619430.1:c.349-5844G>T ENSP00000478572.1:n.349-5844G>T
NM_000062.2:c.737G>T , LRG_105t1:c.737G>T NP_000053.2:p.Ser246Ile
NM_001032295.1:c.737G>T NP_001027466.1:p.Ser246Ile
NM_000062.3:c.737G>T MANE Select NP_000053.2:p.Ser246Ile
NM_001032295.2:c.737G>T NP_001027466.1:p.Ser246Ile