Canonical Allele Identifier: CA380690901

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382017C>T (hg19) ; chr11:g.57614544C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614544C>T , CM000673.2:g.57614544C>T	GRCh38
NC_000011.9:g.57382017C>T , CM000673.1:g.57382017C>T	GRCh37
NC_000011.8:g.57138593C>T	NCBI36
NG_009625.1:g.21991C>T , LRG_105:g.21991C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1466C>T MANE Select	ENSP00000278407.4:p.Pro489Leu
ENST00000528996.2:c.*363C>T	ENSP00000431226.2:n.*363C>T
ENST00000531605.2:c.*1242C>T	ENSP00000503752.1:n.*1242C>T
ENST00000619430.2:c.1262C>T	ENSP00000478572.2:p.Pro421Leu
ENST00000676670.1:c.1466C>T	ENSP00000504807.1:p.Pro489Leu
ENST00000676741.1:n.2548C>T
ENST00000677624.1:c.*886C>T	ENSP00000503979.1:n.*886C>T
ENST00000677625.1:c.1412C>T	ENSP00000502857.1:p.Pro471Leu
ENST00000677856.1:n.1719C>T
ENST00000677915.1:c.*363C>T	ENSP00000503118.1:n.*363C>T
ENST00000678533.1:c.*1020C>T	ENSP00000503873.1:n.*1020C>T
ENST00000678592.1:c.*406C>T	ENSP00000504424.1:n.*406C>T
ENST00000278407.8:c.1466C>T	ENSP00000278407.4:p.Pro489Leu
ENST00000340687.10:c.1355C>T	ENSP00000341861.6:p.Pro452Leu
ENST00000378323.8:c.1481C>T	ENSP00000367574.4:p.Pro494Leu
ENST00000378324.6:c.1310C>T	ENSP00000367575.2:p.Pro437Leu
ENST00000403558.1:c.1595C>T	ENSP00000384420.1:p.Pro532Leu
ENST00000528996.1:c.667C>T	ENSP00000431226.1:n.667C>T
ENST00000531133.5:c.967C>T	ENSP00000435431.1:n.967C>T
ENST00000531797.5:c.*491C>T	ENSP00000432554.1:n.*491C>T
ENST00000619430.1:c.597C>T	ENSP00000478572.1:n.597C>T
NM_000062.2:c.1466C>T , LRG_105t1:c.1466C>T	NP_000053.2:p.Pro489Leu
NM_001032295.1:c.1466C>T	NP_001027466.1:p.Pro489Leu
NM_000062.3:c.1466C>T MANE Select	NP_000053.2:p.Pro489Leu
NM_001032295.2:c.1466C>T	NP_001027466.1:p.Pro489Leu