Canonical Allele Identifier: CA1975531576

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606196A= , CM000673.2:g.57606196A=	GRCh38
NC_000011.9:g.57373669A= , CM000673.1:g.57373669A=	GRCh37
NC_000011.8:g.57130245A=	NCBI36
NG_009625.1:g.13643A= , LRG_105:g.13643A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.872A= MANE Select	ENSP00000278407.4:p.Asn291=
ENST00000528996.2:c.59-5530A=	ENSP00000431226.2:n.59-5530A=
ENST00000531605.2:c.*648A=	ENSP00000503752.1:n.*648A=
ENST00000619430.2:c.686-212A=	ENSP00000478572.2:n.686-212A=
ENST00000676670.1:c.872A=	ENSP00000504807.1:p.Asn291=
ENST00000676741.1:n.1954A=
ENST00000677624.1:c.*292A=	ENSP00000503979.1:n.*292A=
ENST00000677625.1:c.872A=	ENSP00000502857.1:p.Asn291=
ENST00000677856.1:n.931A=
ENST00000677915.1:c.685+4027A=	ENSP00000503118.1:n.685+4027A=
ENST00000678533.1:c.*426A=	ENSP00000503873.1:n.*426A=
ENST00000678592.1:c.872A=	ENSP00000504424.1:p.Asn291=
ENST00000278407.8:c.872A=	ENSP00000278407.4:p.Asn291=
ENST00000340687.10:c.872A=	ENSP00000341861.6:p.Asn291=
ENST00000378323.8:c.887A=	ENSP00000367574.4:p.Asn296=
ENST00000378324.6:c.716A=	ENSP00000367575.2:p.Asn239=
ENST00000403558.1:c.974A=	ENSP00000384420.1:p.Asn325=
ENST00000531133.5:c.373A=	ENSP00000435431.1:n.373A=
ENST00000531797.5:c.*54+4027A=	ENSP00000432554.1:n.*54+4027A=
ENST00000619430.1:c.349-5709A=	ENSP00000478572.1:n.349-5709A=
NM_000062.2:c.872A= , LRG_105t1:c.872A=	NP_000053.2:p.Asn291=
NM_001032295.1:c.872A=	NP_001027466.1:p.Asn291=
NM_000062.3:c.872A= MANE Select	NP_000053.2:p.Asn291=
NM_001032295.2:c.872A=	NP_001027466.1:p.Asn291=