Canonical Allele Identifier: CA16606256
Gene: SERPING1 HGNC NCBI

Linked Data

ClinVar Variation Id: 378573
dbSNP Id: rs1057520366

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.57606195A>C , CM000673.2:g.57606195A>C GRCh38
NC_000011.9:g.57373668A>C , CM000673.1:g.57373668A>C GRCh37
NC_000011.8:g.57130244A>C NCBI36
NG_009625.1:g.13642A>C , LRG_105:g.13642A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000278407.9:c.871A>C MANE Select ENSP00000278407.4:p.Asn291His
ENST00000528996.2:c.59-5531A>C ENSP00000431226.2:n.59-5531A>C
ENST00000531605.2:c.*647A>C ENSP00000503752.1:n.*647A>C
ENST00000619430.2:c.686-213A>C ENSP00000478572.2:n.686-213A>C
ENST00000676670.1:c.871A>C ENSP00000504807.1:p.Asn291His
ENST00000676741.1:n.1953A>C
ENST00000677624.1:c.*291A>C ENSP00000503979.1:n.*291A>C
ENST00000677625.1:c.871A>C ENSP00000502857.1:p.Asn291His
ENST00000677856.1:n.930A>C
ENST00000677915.1:c.685+4026A>C ENSP00000503118.1:n.685+4026A>C
ENST00000678533.1:c.*425A>C ENSP00000503873.1:n.*425A>C
ENST00000678592.1:c.871A>C ENSP00000504424.1:p.Asn291His
ENST00000278407.8:c.871A>C ENSP00000278407.4:p.Asn291His
ENST00000340687.10:c.871A>C ENSP00000341861.6:p.Asn291His
ENST00000378323.8:c.886A>C ENSP00000367574.4:p.Asn296His
ENST00000378324.6:c.715A>C ENSP00000367575.2:p.Asn239His
ENST00000403558.1:c.973A>C ENSP00000384420.1:p.Asn325His
ENST00000531133.5:c.372A>C ENSP00000435431.1:n.372A>C
ENST00000531797.5:c.*54+4026A>C ENSP00000432554.1:n.*54+4026A>C
ENST00000619430.1:c.349-5710A>C ENSP00000478572.1:n.349-5710A>C
NM_000062.2:c.871A>C , LRG_105t1:c.871A>C NP_000053.2:p.Asn291His
NM_001032295.1:c.871A>C NP_001027466.1:p.Asn291His
NM_000062.3:c.871A>C MANE Select NP_000053.2:p.Asn291His
NM_001032295.2:c.871A>C NP_001027466.1:p.Asn291His