Canonical Allele Identifier: CA474806969

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382033A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614560A>C , CM000673.2:g.57614560A>C	GRCh38
NC_000011.9:g.57382033A>C , CM000673.1:g.57382033A>C	GRCh37
NC_000011.8:g.57138609A>C	NCBI36
NG_009625.1:g.22007A>C , LRG_105:g.22007A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1482A>C MANE Select	ENSP00000278407.4:p.Arg494=
ENST00000528996.2:c.*379A>C	ENSP00000431226.2:n.*379A>C
ENST00000531605.2:c.*1258A>C	ENSP00000503752.1:n.*1258A>C
ENST00000619430.2:c.1278A>C	ENSP00000478572.2:p.Arg426=
ENST00000676670.1:c.1482A>C	ENSP00000504807.1:p.Arg494=
ENST00000676741.1:n.2564A>C
ENST00000677624.1:c.*902A>C	ENSP00000503979.1:n.*902A>C
ENST00000677625.1:c.1428A>C	ENSP00000502857.1:p.Arg476=
ENST00000677856.1:n.1735A>C
ENST00000677915.1:c.*379A>C	ENSP00000503118.1:n.*379A>C
ENST00000678533.1:c.*1036A>C	ENSP00000503873.1:n.*1036A>C
ENST00000678592.1:c.*422A>C	ENSP00000504424.1:n.*422A>C
ENST00000278407.8:c.1482A>C	ENSP00000278407.4:p.Arg494=
ENST00000340687.10:c.1371A>C	ENSP00000341861.6:p.Arg457=
ENST00000378323.8:c.1497A>C	ENSP00000367574.4:p.Arg499=
ENST00000378324.6:c.1326A>C	ENSP00000367575.2:p.Arg442=
ENST00000403558.1:c.1611A>C	ENSP00000384420.1:p.Arg537=
ENST00000528996.1:c.683A>C	ENSP00000431226.1:n.683A>C
ENST00000531133.5:c.983A>C	ENSP00000435431.1:n.983A>C
ENST00000531797.5:c.*507A>C	ENSP00000432554.1:n.*507A>C
ENST00000619430.1:c.613A>C	ENSP00000478572.1:n.613A>C
NM_000062.2:c.1482A>C , LRG_105t1:c.1482A>C	NP_000053.2:p.Arg494=
NM_001032295.1:c.1482A>C	NP_001027466.1:p.Arg494=
NM_000062.3:c.1482A>C MANE Select	NP_000053.2:p.Arg494=
NM_001032295.2:c.1482A>C	NP_001027466.1:p.Arg494=