Canonical Allele Identifier: CA380690949

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382041A>C (hg19) ; chr11:g.57614568A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614568A>C , CM000673.2:g.57614568A>C	GRCh38
NC_000011.9:g.57382041A>C , CM000673.1:g.57382041A>C	GRCh37
NC_000011.8:g.57138617A>C	NCBI36
NG_009625.1:g.22015A>C , LRG_105:g.22015A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1490A>C MANE Select	ENSP00000278407.4:p.Asp497Ala
ENST00000528996.2:c.*387A>C	ENSP00000431226.2:n.*387A>C
ENST00000531605.2:c.*1266A>C	ENSP00000503752.1:n.*1266A>C
ENST00000619430.2:c.1286A>C	ENSP00000478572.2:p.Asp429Ala
ENST00000676670.1:c.1490A>C	ENSP00000504807.1:p.Asp497Ala
ENST00000676741.1:n.2572A>C
ENST00000677624.1:c.*910A>C	ENSP00000503979.1:n.*910A>C
ENST00000677625.1:c.1436A>C	ENSP00000502857.1:p.Asp479Ala
ENST00000677856.1:n.1743A>C
ENST00000677915.1:c.*387A>C	ENSP00000503118.1:n.*387A>C
ENST00000678533.1:c.*1044A>C	ENSP00000503873.1:n.*1044A>C
ENST00000678592.1:c.*430A>C	ENSP00000504424.1:n.*430A>C
ENST00000278407.8:c.1490A>C	ENSP00000278407.4:p.Asp497Ala
ENST00000340687.10:c.1379A>C	ENSP00000341861.6:p.Asp460Ala
ENST00000378323.8:c.1505A>C	ENSP00000367574.4:p.Asp502Ala
ENST00000378324.6:c.1334A>C	ENSP00000367575.2:p.Asp445Ala
ENST00000403558.1:c.1619A>C	ENSP00000384420.1:p.Asp540Ala
ENST00000528996.1:c.691A>C	ENSP00000431226.1:n.691A>C
ENST00000531133.5:c.991A>C	ENSP00000435431.1:n.991A>C
ENST00000531797.5:c.*515A>C	ENSP00000432554.1:n.*515A>C
ENST00000619430.1:c.621A>C	ENSP00000478572.1:n.621A>C
NM_000062.2:c.1490A>C , LRG_105t1:c.1490A>C	NP_000053.2:p.Asp497Ala
NM_001032295.1:c.1490A>C	NP_001027466.1:p.Asp497Ala
NM_000062.3:c.1490A>C MANE Select	NP_000053.2:p.Asp497Ala
NM_001032295.2:c.1490A>C	NP_001027466.1:p.Asp497Ala