Canonical Allele Identifier: CA474566577
Gene: SERPING1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.57373607C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606134C>A , CM000673.2:g.57606134C>A GRCh38
NC_000011.9:g.57373607C>A , CM000673.1:g.57373607C>A GRCh37
NC_000011.8:g.57130183C>A NCBI36
NG_009625.1:g.13581C>A , LRG_105:g.13581C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.810C>A MANE Select ENSP00000278407.4:p.Thr270=
ENST00000528996.2:c.59-5592C>A ENSP00000431226.2:n.59-5592C>A
ENST00000531605.2:c.*586C>A ENSP00000503752.1:n.*586C>A
ENST00000619430.2:c.686-274C>A ENSP00000478572.2:n.686-274C>A
ENST00000676670.1:c.810C>A ENSP00000504807.1:p.Thr270=
ENST00000676741.1:n.1892C>A
ENST00000677624.1:c.*230C>A ENSP00000503979.1:n.*230C>A
ENST00000677625.1:c.810C>A ENSP00000502857.1:p.Thr270=
ENST00000677856.1:n.869C>A
ENST00000677915.1:c.685+3965C>A ENSP00000503118.1:n.685+3965C>A
ENST00000678533.1:c.*364C>A ENSP00000503873.1:n.*364C>A
ENST00000678592.1:c.810C>A ENSP00000504424.1:p.Thr270=
ENST00000278407.8:c.810C>A ENSP00000278407.4:p.Thr270=
ENST00000340687.10:c.810C>A ENSP00000341861.6:p.Thr270=
ENST00000378323.8:c.825C>A ENSP00000367574.4:p.Thr275=
ENST00000378324.6:c.654C>A ENSP00000367575.2:p.Thr218=
ENST00000403558.1:c.912C>A ENSP00000384420.1:p.Thr304=
ENST00000531133.5:c.311C>A ENSP00000435431.1:n.311C>A
ENST00000531797.5:c.*54+3965C>A ENSP00000432554.1:n.*54+3965C>A
ENST00000619430.1:c.349-5771C>A ENSP00000478572.1:n.349-5771C>A
NM_000062.2:c.810C>A , LRG_105t1:c.810C>A NP_000053.2:p.Thr270=
NM_001032295.1:c.810C>A NP_001027466.1:p.Thr270=
NM_000062.3:c.810C>A MANE Select NP_000053.2:p.Thr270=
NM_001032295.2:c.810C>A NP_001027466.1:p.Thr270=