Canonical Allele Identifier: CA1975539263
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57614483C= , CM000673.2:g.57614483C= GRCh38
NC_000011.9:g.57381956C= , CM000673.1:g.57381956C= GRCh37
NC_000011.8:g.57138532C= NCBI36
NG_009625.1:g.21930C= , LRG_105:g.21930C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1405C= MANE Select ENSP00000278407.4:p.Leu469=
ENST00000528996.2:c.*302C= ENSP00000431226.2:n.*302C=
ENST00000531605.2:c.*1181C= ENSP00000503752.1:n.*1181C=
ENST00000619430.2:c.1201C= ENSP00000478572.2:p.Leu401=
ENST00000676670.1:c.1405C= ENSP00000504807.1:p.Leu469=
ENST00000676741.1:n.2487C=
ENST00000677624.1:c.*825C= ENSP00000503979.1:n.*825C=
ENST00000677625.1:c.1351C= ENSP00000502857.1:p.Leu451=
ENST00000677856.1:n.1658C=
ENST00000677915.1:c.*302C= ENSP00000503118.1:n.*302C=
ENST00000678533.1:c.*959C= ENSP00000503873.1:n.*959C=
ENST00000678592.1:c.*345C= ENSP00000504424.1:n.*345C=
ENST00000278407.8:c.1405C= ENSP00000278407.4:p.Leu469=
ENST00000340687.10:c.1294C= ENSP00000341861.6:p.Leu432=
ENST00000378323.8:c.1420C= ENSP00000367574.4:p.Leu474=
ENST00000378324.6:c.1249C= ENSP00000367575.2:p.Leu417=
ENST00000403558.1:c.1534C= ENSP00000384420.1:p.Leu512=
ENST00000528996.1:c.606C= ENSP00000431226.1:n.606C=
ENST00000530113.1:n.862C=
ENST00000531133.5:c.906C= ENSP00000435431.1:n.906C=
ENST00000531797.5:c.*430C= ENSP00000432554.1:n.*430C=
ENST00000619430.1:c.536C= ENSP00000478572.1:n.536C=
NM_000062.2:c.1405C= , LRG_105t1:c.1405C= NP_000053.2:p.Leu469=
NM_001032295.1:c.1405C= NP_001027466.1:p.Leu469=
NM_000062.3:c.1405C= MANE Select NP_000053.2:p.Leu469=
NM_001032295.2:c.1405C= NP_001027466.1:p.Leu469=