Canonical Allele Identifier: CA1975537145
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611865C= , CM000673.2:g.57611865C= GRCh38
NC_000011.9:g.57379338C= , CM000673.1:g.57379338C= GRCh37
NC_000011.8:g.57135914C= NCBI36
NG_009625.1:g.19312C= , LRG_105:g.19312C=

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.1178C= MANE Select ENSP00000278407.4:p.Pro393=
ENST00000528996.2:c.*75C= ENSP00000431226.2:n.*75C=
ENST00000531605.2:c.*954C= ENSP00000503752.1:n.*954C=
ENST00000619430.2:c.974C= ENSP00000478572.2:p.Pro325=
ENST00000676670.1:c.1178C= ENSP00000504807.1:p.Pro393=
ENST00000676741.1:n.2260C=
ENST00000677624.1:c.*598C= ENSP00000503979.1:n.*598C=
ENST00000677625.1:c.1124C= ENSP00000502857.1:p.Pro375=
ENST00000677856.1:n.1431C=
ENST00000677915.1:c.*75C= ENSP00000503118.1:n.*75C=
ENST00000678533.1:c.*732C= ENSP00000503873.1:n.*732C=
ENST00000678592.1:c.*118C= ENSP00000504424.1:n.*118C=
ENST00000278407.8:c.1178C= ENSP00000278407.4:p.Pro393=
ENST00000340687.10:c.1067C= ENSP00000341861.6:p.Pro356=
ENST00000378323.8:c.1193C= ENSP00000367574.4:p.Pro398=
ENST00000378324.6:c.1022C= ENSP00000367575.2:p.Pro341=
ENST00000403558.1:c.1307C= ENSP00000384420.1:p.Pro436=
ENST00000528996.1:c.379C= ENSP00000431226.1:n.379C=
ENST00000530113.1:n.635C=
ENST00000531133.5:c.679C= ENSP00000435431.1:n.679C=
ENST00000531797.5:c.*203C= ENSP00000432554.1:n.*203C=
ENST00000619430.1:c.349-40C= ENSP00000478572.1:n.349-40C=
NM_000062.2:c.1178C= , LRG_105t1:c.1178C= NP_000053.2:p.Pro393=
NM_001032295.1:c.1178C= NP_001027466.1:p.Pro393=
NM_000062.3:c.1178C= MANE Select NP_000053.2:p.Pro393=
NM_001032295.2:c.1178C= NP_001027466.1:p.Pro393=