Canonical Allele Identifier: CA1975532524

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606859T= , CM000673.2:g.57606859T=	GRCh38
NC_000011.9:g.57374332T= , CM000673.1:g.57374332T=	GRCh37
NC_000011.8:g.57130908T=	NCBI36
NG_009625.1:g.14306T= , LRG_105:g.14306T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000062.3:c.1029+312T= MANE Select	NP_000053.2:n.1029+312T=
ENST00000278407.9:c.1029+312T= MANE Select	ENSP00000278407.4:n.1029+312T=
NM_000062.2:c.1029+312T= , LRG_105t1:c.1029+312T=	NP_000053.2:n.1029+312T=
NM_001032295.1:c.1029+312T=	NP_001027466.1:n.1029+312T=
NM_001032295.2:c.1029+312T=	NP_001027466.1:n.1029+312T=
ENST00000278407.8:c.1029+312T=	ENSP00000278407.4:n.1029+312T=
ENST00000340687.10:c.1029+312T=	ENSP00000341861.6:n.1029+312T=
ENST00000378323.8:c.1044+312T=	ENSP00000367574.4:n.1044+312T=
ENST00000378324.6:c.873+312T=	ENSP00000367575.2:n.873+312T=
ENST00000403558.1:c.1158+312T=	ENSP00000384420.1:n.1158+312T=
ENST00000528996.1:c.230+60T=	ENSP00000431226.1:n.230+60T=
ENST00000528996.2:c.59-4867T=	ENSP00000431226.2:n.59-4867T=
ENST00000531133.5:c.530+312T=	ENSP00000435431.1:n.530+312T=
ENST00000531605.2:c.*805+312T=	ENSP00000503752.1:n.*805+312T=
ENST00000531797.5:c.*54+4690T=	ENSP00000432554.1:n.*54+4690T=
ENST00000619430.1:c.349-5046T=	ENSP00000478572.1:n.349-5046T=
ENST00000619430.2:c.825+312T=	ENSP00000478572.2:n.825+312T=
ENST00000676670.1:c.1029+312T=	ENSP00000504807.1:n.1029+312T=
ENST00000676741.1:n.2111+312T=
ENST00000677624.1:c.*449+312T=	ENSP00000503979.1:n.*449+312T=
ENST00000677625.1:c.1029+312T=	ENSP00000502857.1:n.1029+312T=
ENST00000677856.1:n.1282+312T=
ENST00000677915.1:c.685+4690T=	ENSP00000503118.1:n.685+4690T=
ENST00000678533.1:c.*583+312T=	ENSP00000503873.1:n.*583+312T=
ENST00000678592.1:c.1118+60T=	ENSP00000504424.1:n.1118+60T=