Canonical Allele Identifier: CA1975536167
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57610865C= , CM000673.2:g.57610865C= GRCh38
NC_000011.9:g.57378338C= , CM000673.1:g.57378338C= GRCh37
NC_000011.8:g.57134914C= NCBI36
NG_009625.1:g.18312C= , LRG_105:g.18312C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1030-852C= MANE Select ENSP00000278407.4:n.1030-852C=
ENST00000528996.2:c.59-861C= ENSP00000431226.2:n.59-861C=
ENST00000531605.2:c.*806-852C= ENSP00000503752.1:n.*806-852C=
ENST00000619430.2:c.826-852C= ENSP00000478572.2:n.826-852C=
ENST00000676670.1:c.1030-852C= ENSP00000504807.1:n.1030-852C=
ENST00000676741.1:n.2112-852C=
ENST00000677624.1:c.*450-852C= ENSP00000503979.1:n.*450-852C=
ENST00000677625.1:c.1030-906C= ENSP00000502857.1:n.1030-906C=
ENST00000677856.1:n.1283-852C=
ENST00000677915.1:c.686-852C= ENSP00000503118.1:n.686-852C=
ENST00000678533.1:c.*584-852C= ENSP00000503873.1:n.*584-852C=
ENST00000678592.1:c.1119-852C= ENSP00000504424.1:n.1119-852C=
ENST00000278407.8:c.1030-852C= ENSP00000278407.4:n.1030-852C=
ENST00000340687.10:c.1030-963C= ENSP00000341861.6:n.1030-963C=
ENST00000378323.8:c.1045-852C= ENSP00000367574.4:n.1045-852C=
ENST00000378324.6:c.874-852C= ENSP00000367575.2:n.874-852C=
ENST00000403558.1:c.1159-852C= ENSP00000384420.1:n.1159-852C=
ENST00000528996.1:c.231-852C= ENSP00000431226.1:n.231-852C=
ENST00000531133.5:c.531-852C= ENSP00000435431.1:n.531-852C=
ENST00000531797.5:c.*55-852C= ENSP00000432554.1:n.*55-852C=
ENST00000619430.1:c.349-1040C= ENSP00000478572.1:n.349-1040C=
NM_000062.2:c.1030-852C= , LRG_105t1:c.1030-852C= NP_000053.2:n.1030-852C=
NM_001032295.1:c.1030-852C= NP_001027466.1:n.1030-852C=
NM_000062.3:c.1030-852C= MANE Select NP_000053.2:n.1030-852C=
NM_001032295.2:c.1030-852C= NP_001027466.1:n.1030-852C=