Canonical Allele Identifier: CA1975539307

Gene: SERPING1

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614516G= , CM000673.2:g.57614516G=	GRCh38
NC_000011.9:g.57381989G= , CM000673.1:g.57381989G=	GRCh37
NC_000011.8:g.57138565G=	NCBI36
NG_009625.1:g.21963G= , LRG_105:g.21963G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1438G= MANE Select	ENSP00000278407.4:p.Val480=
ENST00000528996.2:c.*335G=	ENSP00000431226.2:n.*335G=
ENST00000531605.2:c.*1214G=	ENSP00000503752.1:n.*1214G=
ENST00000619430.2:c.1234G=	ENSP00000478572.2:p.Val412=
ENST00000676670.1:c.1438G=	ENSP00000504807.1:p.Val480=
ENST00000676741.1:n.2520G=
ENST00000677624.1:c.*858G=	ENSP00000503979.1:n.*858G=
ENST00000677625.1:c.1384G=	ENSP00000502857.1:p.Val462=
ENST00000677856.1:n.1691G=
ENST00000677915.1:c.*335G=	ENSP00000503118.1:n.*335G=
ENST00000678533.1:c.*992G=	ENSP00000503873.1:n.*992G=
ENST00000678592.1:c.*378G=	ENSP00000504424.1:n.*378G=
ENST00000278407.8:c.1438G=	ENSP00000278407.4:p.Val480=
ENST00000340687.10:c.1327G=	ENSP00000341861.6:p.Val443=
ENST00000378323.8:c.1453G=	ENSP00000367574.4:p.Val485=
ENST00000378324.6:c.1282G=	ENSP00000367575.2:p.Val428=
ENST00000403558.1:c.1567G=	ENSP00000384420.1:p.Val523=
ENST00000528996.1:c.639G=	ENSP00000431226.1:n.639G=
ENST00000530113.1:n.895G=
ENST00000531133.5:c.939G=	ENSP00000435431.1:n.939G=
ENST00000531797.5:c.*463G=	ENSP00000432554.1:n.*463G=
ENST00000619430.1:c.569G=	ENSP00000478572.1:n.569G=
NM_000062.2:c.1438G= , LRG_105t1:c.1438G=	NP_000053.2:p.Val480=
NM_001032295.1:c.1438G=	NP_001027466.1:p.Val480=
NM_000062.3:c.1438G= MANE Select	NP_000053.2:p.Val480=
NM_001032295.2:c.1438G=	NP_001027466.1:p.Val480=