Canonical Allele Identifier: CA380702838
Gene: SERPING1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57611811G>A , CM000673.2:g.57611811G>A GRCh38
NC_000011.9:g.57379284G>A , CM000673.1:g.57379284G>A GRCh37
NC_000011.8:g.57135860G>A NCBI36
NG_009625.1:g.19258G>A , LRG_105:g.19258G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000278407.9:c.1124G>A MANE Select ENSP00000278407.4:p.Ser375Asn
ENST00000528996.2:c.*21G>A ENSP00000431226.2:n.*21G>A
ENST00000531605.2:c.*900G>A ENSP00000503752.1:n.*900G>A
ENST00000619430.2:c.920G>A ENSP00000478572.2:p.Ser307Asn
ENST00000676670.1:c.1124G>A ENSP00000504807.1:p.Ser375Asn
ENST00000676741.1:n.2206G>A
ENST00000677624.1:c.*544G>A ENSP00000503979.1:n.*544G>A
ENST00000677625.1:c.1070G>A ENSP00000502857.1:p.Ser357Asn
ENST00000677856.1:n.1377G>A
ENST00000677915.1:c.*21G>A ENSP00000503118.1:n.*21G>A
ENST00000678533.1:c.*678G>A ENSP00000503873.1:n.*678G>A
ENST00000678592.1:c.*64G>A ENSP00000504424.1:n.*64G>A
ENST00000278407.8:c.1124G>A ENSP00000278407.4:p.Ser375Asn
ENST00000340687.10:c.1030-17G>A ENSP00000341861.6:n.1030-17G>A
ENST00000378323.8:c.1139G>A ENSP00000367574.4:p.Ser380Asn
ENST00000378324.6:c.968G>A ENSP00000367575.2:p.Ser323Asn
ENST00000403558.1:c.1253G>A ENSP00000384420.1:p.Ser418Asn
ENST00000528996.1:c.325G>A ENSP00000431226.1:n.325G>A
ENST00000530113.1:n.581G>A
ENST00000531133.5:c.625G>A ENSP00000435431.1:n.625G>A
ENST00000531797.5:c.*149G>A ENSP00000432554.1:n.*149G>A
ENST00000619430.1:c.349-94G>A ENSP00000478572.1:n.349-94G>A
NM_000062.2:c.1124G>A , LRG_105t1:c.1124G>A NP_000053.2:p.Ser375Asn
NM_001032295.1:c.1124G>A NP_001027466.1:p.Ser375Asn
NM_000062.3:c.1124G>A MANE Select NP_000053.2:p.Ser375Asn
NM_001032295.2:c.1124G>A NP_001027466.1:p.Ser375Asn