Canonical Allele Identifier: CA6008209
Gene: SERPING1 HGNC NCBI

Linked Data

dbSNP Id: rs746674351

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611678C>A , CM000673.2:g.57611678C>A GRCh38
NC_000011.9:g.57379151C>A , CM000673.1:g.57379151C>A GRCh37
NC_000011.8:g.57135727C>A NCBI36
NG_009625.1:g.19125C>A , LRG_105:g.19125C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1030-39C>A MANE Select ENSP00000278407.4:n.1030-39C>A
ENST00000528996.2:c.59-48C>A ENSP00000431226.2:n.59-48C>A
ENST00000531605.2:c.*806-39C>A ENSP00000503752.1:n.*806-39C>A
ENST00000619430.2:c.826-39C>A ENSP00000478572.2:n.826-39C>A
ENST00000676670.1:c.1030-39C>A ENSP00000504807.1:n.1030-39C>A
ENST00000676741.1:n.2112-39C>A
ENST00000677624.1:c.*450-39C>A ENSP00000503979.1:n.*450-39C>A
ENST00000677625.1:c.1030-93C>A ENSP00000502857.1:n.1030-93C>A
ENST00000677856.1:n.1283-39C>A
ENST00000677915.1:c.686-39C>A ENSP00000503118.1:n.686-39C>A
ENST00000678533.1:c.*584-39C>A ENSP00000503873.1:n.*584-39C>A
ENST00000678592.1:c.1119-39C>A ENSP00000504424.1:n.1119-39C>A
ENST00000278407.8:c.1030-39C>A ENSP00000278407.4:n.1030-39C>A
ENST00000340687.10:c.1030-150C>A ENSP00000341861.6:n.1030-150C>A
ENST00000378323.8:c.1045-39C>A ENSP00000367574.4:n.1045-39C>A
ENST00000378324.6:c.874-39C>A ENSP00000367575.2:n.874-39C>A
ENST00000403558.1:c.1159-39C>A ENSP00000384420.1:n.1159-39C>A
ENST00000528996.1:c.231-39C>A ENSP00000431226.1:n.231-39C>A
ENST00000530113.1:n.448C>A
ENST00000531133.5:c.531-39C>A ENSP00000435431.1:n.531-39C>A
ENST00000531797.5:c.*55-39C>A ENSP00000432554.1:n.*55-39C>A
ENST00000619430.1:c.349-227C>A ENSP00000478572.1:n.349-227C>A
NM_000062.2:c.1030-39C>A , LRG_105t1:c.1030-39C>A NP_000053.2:n.1030-39C>A
NM_001032295.1:c.1030-39C>A NP_001027466.1:n.1030-39C>A
NM_000062.3:c.1030-39C>A MANE Select NP_000053.2:n.1030-39C>A
NM_001032295.2:c.1030-39C>A NP_001027466.1:n.1030-39C>A