Canonical Allele Identifier: CA380690293

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381831T>C (hg19) ; chr11:g.57614358T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614358T>C , CM000673.2:g.57614358T>C	GRCh38
NC_000011.9:g.57381831T>C , CM000673.1:g.57381831T>C	GRCh37
NC_000011.8:g.57138407T>C	NCBI36
NG_009625.1:g.21805T>C , LRG_105:g.21805T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1280T>C MANE Select	ENSP00000278407.4:p.Leu427Pro
ENST00000528996.2:c.*177T>C	ENSP00000431226.2:n.*177T>C
ENST00000531605.2:c.*1056T>C	ENSP00000503752.1:n.*1056T>C
ENST00000619430.2:c.1076T>C	ENSP00000478572.2:p.Leu359Pro
ENST00000676670.1:c.1280T>C	ENSP00000504807.1:p.Leu427Pro
ENST00000676741.1:n.2362T>C
ENST00000677624.1:c.*700T>C	ENSP00000503979.1:n.*700T>C
ENST00000677625.1:c.1226T>C	ENSP00000502857.1:p.Leu409Pro
ENST00000677856.1:n.1533T>C
ENST00000677915.1:c.*177T>C	ENSP00000503118.1:n.*177T>C
ENST00000678533.1:c.*834T>C	ENSP00000503873.1:n.*834T>C
ENST00000678592.1:c.*220T>C	ENSP00000504424.1:n.*220T>C
ENST00000278407.8:c.1280T>C	ENSP00000278407.4:p.Leu427Pro
ENST00000340687.10:c.1169T>C	ENSP00000341861.6:p.Leu390Pro
ENST00000378323.8:c.1295T>C	ENSP00000367574.4:p.Leu432Pro
ENST00000378324.6:c.1124T>C	ENSP00000367575.2:p.Leu375Pro
ENST00000403558.1:c.1409T>C	ENSP00000384420.1:p.Leu470Pro
ENST00000528996.1:c.481T>C	ENSP00000431226.1:n.481T>C
ENST00000530113.1:n.737T>C
ENST00000531133.5:c.781T>C	ENSP00000435431.1:n.781T>C
ENST00000531797.5:c.*305T>C	ENSP00000432554.1:n.*305T>C
ENST00000619430.1:c.411T>C	ENSP00000478572.1:n.411T>C
NM_000062.2:c.1280T>C , LRG_105t1:c.1280T>C	NP_000053.2:p.Leu427Pro
NM_001032295.1:c.1280T>C	NP_001027466.1:p.Leu427Pro
NM_000062.3:c.1280T>C MANE Select	NP_000053.2:p.Leu427Pro
NM_001032295.2:c.1280T>C	NP_001027466.1:p.Leu427Pro