Canonical Allele Identifier: CA1975536869
Gene: SERPING1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611742A= , CM000673.2:g.57611742A= GRCh38
NC_000011.9:g.57379215A= , CM000673.1:g.57379215A= GRCh37
NC_000011.8:g.57135791A= NCBI36
NG_009625.1:g.19189A= , LRG_105:g.19189A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1055A= MANE Select ENSP00000278407.4:p.Asn352=
ENST00000528996.2:c.75A= ENSP00000431226.2:p.Gln25=
ENST00000531605.2:c.*831A= ENSP00000503752.1:n.*831A=
ENST00000619430.2:c.851A= ENSP00000478572.2:p.Asn284=
ENST00000676670.1:c.1055A= ENSP00000504807.1:p.Asn352=
ENST00000676741.1:n.2137A=
ENST00000677624.1:c.*475A= ENSP00000503979.1:n.*475A=
ENST00000677625.1:c.1030-29A= ENSP00000502857.1:n.1030-29A=
ENST00000677856.1:n.1308A=
ENST00000677915.1:c.711A= ENSP00000503118.1:p.Gln237=
ENST00000678533.1:c.*609A= ENSP00000503873.1:n.*609A=
ENST00000678592.1:c.1144A= ENSP00000504424.1:p.Ile382=
ENST00000278407.8:c.1055A= ENSP00000278407.4:p.Asn352=
ENST00000340687.10:c.1030-86A= ENSP00000341861.6:n.1030-86A=
ENST00000378323.8:c.1070A= ENSP00000367574.4:p.Asn357=
ENST00000378324.6:c.899A= ENSP00000367575.2:p.Asn300=
ENST00000403558.1:c.1184A= ENSP00000384420.1:p.Asn395=
ENST00000528996.1:c.256A= ENSP00000431226.1:p.Ile86=
ENST00000530113.1:n.512A=
ENST00000531133.5:c.556A= ENSP00000435431.1:n.556A=
ENST00000531797.5:c.*80A= ENSP00000432554.1:n.*80A=
ENST00000619430.1:c.349-163A= ENSP00000478572.1:n.349-163A=
NM_000062.2:c.1055A= , LRG_105t1:c.1055A= NP_000053.2:p.Asn352=
NM_001032295.1:c.1055A= NP_001027466.1:p.Asn352=
NM_000062.3:c.1055A= MANE Select NP_000053.2:p.Asn352=
NM_001032295.2:c.1055A= NP_001027466.1:p.Asn352=