Canonical Allele Identifier: CA2613601949
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57601987C>A , CM000673.2:g.57601987C>A GRCh38
NC_000011.9:g.57369460C>A , CM000673.1:g.57369460C>A GRCh37
NC_000011.8:g.57126036C>A NCBI36
NG_009625.1:g.9434C>A , LRG_105:g.9434C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.551-48C>A MANE Select ENSP00000278407.4:n.551-48C>A
ENST00000528996.2:c.58+3659C>A ENSP00000431226.2:n.58+3659C>A
ENST00000531605.2:c.52-48C>A ENSP00000503752.1:n.52-48C>A
ENST00000619430.2:c.551-48C>A ENSP00000478572.2:n.551-48C>A
ENST00000676670.1:c.551-48C>A ENSP00000504807.1:n.551-48C>A
ENST00000676741.1:n.1633-48C>A
ENST00000677275.1:n.538-48C>A
ENST00000677624.1:c.551-48C>A ENSP00000503979.1:n.551-48C>A
ENST00000677625.1:c.551-48C>A ENSP00000502857.1:n.551-48C>A
ENST00000677856.1:n.610-48C>A
ENST00000677915.1:c.551-48C>A ENSP00000503118.1:n.551-48C>A
ENST00000678533.1:c.52-48C>A ENSP00000503873.1:n.52-48C>A
ENST00000678592.1:c.551-48C>A ENSP00000504424.1:n.551-48C>A
ENST00000278407.8:c.551-48C>A ENSP00000278407.4:n.551-48C>A
ENST00000340687.10:c.551-48C>A ENSP00000341861.6:n.551-48C>A
ENST00000378323.8:c.566-48C>A ENSP00000367574.4:n.566-48C>A
ENST00000378324.6:c.395-48C>A ENSP00000367575.2:n.395-48C>A
ENST00000403558.1:c.653-48C>A ENSP00000384420.1:n.653-48C>A
ENST00000531133.5:c.52-48C>A ENSP00000435431.1:n.52-48C>A
ENST00000531797.5:c.52-48C>A ENSP00000432554.1:n.52-48C>A
ENST00000619430.1:c.348+1812C>A ENSP00000478572.1:n.348+1812C>A
NM_000062.2:c.551-48C>A , LRG_105t1:c.551-48C>A NP_000053.2:n.551-48C>A
NM_001032295.1:c.551-48C>A NP_001027466.1:n.551-48C>A
NM_000062.3:c.551-48C>A MANE Select NP_000053.2:n.551-48C>A
NM_001032295.2:c.551-48C>A NP_001027466.1:n.551-48C>A