Canonical Allele Identifier: CA1975531556

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606188C= , CM000673.2:g.57606188C=	GRCh38
NC_000011.9:g.57373661C= , CM000673.1:g.57373661C=	GRCh37
NC_000011.8:g.57130237C=	NCBI36
NG_009625.1:g.13635C= , LRG_105:g.13635C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.864C= MANE Select	ENSP00000278407.4:p.Val288=
ENST00000528996.2:c.59-5538C=	ENSP00000431226.2:n.59-5538C=
ENST00000531605.2:c.*640C=	ENSP00000503752.1:n.*640C=
ENST00000619430.2:c.686-220C=	ENSP00000478572.2:n.686-220C=
ENST00000676670.1:c.864C=	ENSP00000504807.1:p.Val288=
ENST00000676741.1:n.1946C=
ENST00000677624.1:c.*284C=	ENSP00000503979.1:n.*284C=
ENST00000677625.1:c.864C=	ENSP00000502857.1:p.Val288=
ENST00000677856.1:n.923C=
ENST00000677915.1:c.685+4019C=	ENSP00000503118.1:n.685+4019C=
ENST00000678533.1:c.*418C=	ENSP00000503873.1:n.*418C=
ENST00000678592.1:c.864C=	ENSP00000504424.1:p.Val288=
ENST00000278407.8:c.864C=	ENSP00000278407.4:p.Val288=
ENST00000340687.10:c.864C=	ENSP00000341861.6:p.Val288=
ENST00000378323.8:c.879C=	ENSP00000367574.4:p.Val293=
ENST00000378324.6:c.708C=	ENSP00000367575.2:p.Val236=
ENST00000403558.1:c.966C=	ENSP00000384420.1:p.Val322=
ENST00000531133.5:c.365C=	ENSP00000435431.1:n.365C=
ENST00000531797.5:c.*54+4019C=	ENSP00000432554.1:n.*54+4019C=
ENST00000619430.1:c.349-5717C=	ENSP00000478572.1:n.349-5717C=
NM_000062.2:c.864C= , LRG_105t1:c.864C=	NP_000053.2:p.Val288=
NM_001032295.1:c.864C=	NP_001027466.1:p.Val288=
NM_000062.3:c.864C= MANE Select	NP_000053.2:p.Val288=
NM_001032295.2:c.864C=	NP_001027466.1:p.Val288=