Canonical Allele Identifier: CA1975531331

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606073T= , CM000673.2:g.57606073T=	GRCh38
NC_000011.9:g.57373546T= , CM000673.1:g.57373546T=	GRCh37
NC_000011.8:g.57130122T=	NCBI36
NG_009625.1:g.13520T= , LRG_105:g.13520T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.749T= MANE Select	ENSP00000278407.4:p.Val250=
ENST00000528996.2:c.59-5653T=	ENSP00000431226.2:n.59-5653T=
ENST00000531605.2:c.*525T=	ENSP00000503752.1:n.*525T=
ENST00000619430.2:c.686-335T=	ENSP00000478572.2:n.686-335T=
ENST00000676670.1:c.749T=	ENSP00000504807.1:p.Val250=
ENST00000676741.1:n.1831T=
ENST00000677624.1:c.*169T=	ENSP00000503979.1:n.*169T=
ENST00000677625.1:c.749T=	ENSP00000502857.1:p.Val250=
ENST00000677856.1:n.808T=
ENST00000677915.1:c.685+3904T=	ENSP00000503118.1:n.685+3904T=
ENST00000678533.1:c.*303T=	ENSP00000503873.1:n.*303T=
ENST00000678592.1:c.749T=	ENSP00000504424.1:p.Val250=
ENST00000278407.8:c.749T=	ENSP00000278407.4:p.Val250=
ENST00000340687.10:c.749T=	ENSP00000341861.6:p.Val250=
ENST00000378323.8:c.764T=	ENSP00000367574.4:p.Val255=
ENST00000378324.6:c.593T=	ENSP00000367575.2:p.Val198=
ENST00000403558.1:c.851T=	ENSP00000384420.1:p.Val284=
ENST00000531133.5:c.250T=	ENSP00000435431.1:n.250T=
ENST00000531797.5:c.*54+3904T=	ENSP00000432554.1:n.*54+3904T=
ENST00000619430.1:c.349-5832T=	ENSP00000478572.1:n.349-5832T=
NM_000062.2:c.749T= , LRG_105t1:c.749T=	NP_000053.2:p.Val250=
NM_001032295.1:c.749T=	NP_001027466.1:p.Val250=
NM_000062.3:c.749T= MANE Select	NP_000053.2:p.Val250=
NM_001032295.2:c.749T=	NP_001027466.1:p.Val250=