Canonical Allele Identifier: CA223024339

Gene: SERPING1

Linked Data

• dbSNP Id: rs956390201
• MyVariant Identifiers: chr11:g.57381968G>C (hg19) ; chr11:g.57614495G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614495G>C , CM000673.2:g.57614495G>C	GRCh38
NC_000011.9:g.57381968G>C , CM000673.1:g.57381968G>C	GRCh37
NC_000011.8:g.57138544G>C	NCBI36
NG_009625.1:g.21942G>C , LRG_105:g.21942G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1417G>C MANE Select	ENSP00000278407.4:p.Val473Leu
ENST00000528996.2:c.*314G>C	ENSP00000431226.2:n.*314G>C
ENST00000531605.2:c.*1193G>C	ENSP00000503752.1:n.*1193G>C
ENST00000619430.2:c.1213G>C	ENSP00000478572.2:p.Val405Leu
ENST00000676670.1:c.1417G>C	ENSP00000504807.1:p.Val473Leu
ENST00000676741.1:n.2499G>C
ENST00000677624.1:c.*837G>C	ENSP00000503979.1:n.*837G>C
ENST00000677625.1:c.1363G>C	ENSP00000502857.1:p.Val455Leu
ENST00000677856.1:n.1670G>C
ENST00000677915.1:c.*314G>C	ENSP00000503118.1:n.*314G>C
ENST00000678533.1:c.*971G>C	ENSP00000503873.1:n.*971G>C
ENST00000678592.1:c.*357G>C	ENSP00000504424.1:n.*357G>C
ENST00000278407.8:c.1417G>C	ENSP00000278407.4:p.Val473Leu
ENST00000340687.10:c.1306G>C	ENSP00000341861.6:p.Val436Leu
ENST00000378323.8:c.1432G>C	ENSP00000367574.4:p.Val478Leu
ENST00000378324.6:c.1261G>C	ENSP00000367575.2:p.Val421Leu
ENST00000403558.1:c.1546G>C	ENSP00000384420.1:p.Val516Leu
ENST00000528996.1:c.618G>C	ENSP00000431226.1:n.618G>C
ENST00000530113.1:n.874G>C
ENST00000531133.5:c.918G>C	ENSP00000435431.1:n.918G>C
ENST00000531797.5:c.*442G>C	ENSP00000432554.1:n.*442G>C
ENST00000619430.1:c.548G>C	ENSP00000478572.1:n.548G>C
NM_000062.2:c.1417G>C , LRG_105t1:c.1417G>C	NP_000053.2:p.Val473Leu
NM_001032295.1:c.1417G>C	NP_001027466.1:p.Val473Leu
NM_000062.3:c.1417G>C MANE Select	NP_000053.2:p.Val473Leu
NM_001032295.2:c.1417G>C	NP_001027466.1:p.Val473Leu