Canonical Allele Identifier: CA1975531569
Community Standard Title: NM_000062.3(SERPING1):c.871A= (p.Asn291=)
Gene: SERPING1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NM_000062.3:c.871A= MANE Select NP_000053.2:p.Asn291=
ENST00000278407.9:c.871A= MANE Select ENSP00000278407.4:p.Asn291=
NM_000062.2:c.871A= , LRG_105t1:c.871A= NP_000053.2:p.Asn291=
NM_001032295.1:c.871A= NP_001027466.1:p.Asn291=
NM_001032295.2:c.871A= NP_001027466.1:p.Asn291=
ENST00000278407.8:c.871A= ENSP00000278407.4:p.Asn291=
ENST00000340687.10:c.871A= ENSP00000341861.6:p.Asn291=
ENST00000378323.8:c.886A= ENSP00000367574.4:p.Asn296=
ENST00000378324.6:c.715A= ENSP00000367575.2:p.Asn239=
ENST00000403558.1:c.973A= ENSP00000384420.1:p.Asn325=
ENST00000528996.2:c.59-5531A= ENSP00000431226.2:n.59-5531A=
ENST00000531133.5:c.372A= ENSP00000435431.1:n.372A=
ENST00000531605.2:c.*647A= ENSP00000503752.1:n.*647A=
ENST00000531797.5:c.*54+4026A= ENSP00000432554.1:n.*54+4026A=
ENST00000619430.1:c.349-5710A= ENSP00000478572.1:n.349-5710A=
ENST00000619430.2:c.686-213A= ENSP00000478572.2:n.686-213A=
ENST00000676670.1:c.871A= ENSP00000504807.1:p.Asn291=
ENST00000676741.1:n.1953A=
ENST00000677624.1:c.*291A= ENSP00000503979.1:n.*291A=
ENST00000677625.1:c.871A= ENSP00000502857.1:p.Asn291=
ENST00000677856.1:n.930A=
ENST00000677915.1:c.685+4026A= ENSP00000503118.1:n.685+4026A=
ENST00000678533.1:c.*425A= ENSP00000503873.1:n.*425A=
ENST00000678592.1:c.871A= ENSP00000504424.1:p.Asn291=