Canonical Allele Identifier: CA380703247

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379341C>G (hg19) ; chr11:g.57611868C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611868C>G , CM000673.2:g.57611868C>G	GRCh38
NC_000011.9:g.57379341C>G , CM000673.1:g.57379341C>G	GRCh37
NC_000011.8:g.57135917C>G	NCBI36
NG_009625.1:g.19315C>G , LRG_105:g.19315C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1181C>G MANE Select	ENSP00000278407.4:p.Thr394Ser
ENST00000528996.2:c.*78C>G	ENSP00000431226.2:n.*78C>G
ENST00000531605.2:c.*957C>G	ENSP00000503752.1:n.*957C>G
ENST00000619430.2:c.977C>G	ENSP00000478572.2:p.Thr326Ser
ENST00000676670.1:c.1181C>G	ENSP00000504807.1:p.Thr394Ser
ENST00000676741.1:n.2263C>G
ENST00000677624.1:c.*601C>G	ENSP00000503979.1:n.*601C>G
ENST00000677625.1:c.1127C>G	ENSP00000502857.1:p.Thr376Ser
ENST00000677856.1:n.1434C>G
ENST00000677915.1:c.*78C>G	ENSP00000503118.1:n.*78C>G
ENST00000678533.1:c.*735C>G	ENSP00000503873.1:n.*735C>G
ENST00000678592.1:c.*121C>G	ENSP00000504424.1:n.*121C>G
ENST00000278407.8:c.1181C>G	ENSP00000278407.4:p.Thr394Ser
ENST00000340687.10:c.1070C>G	ENSP00000341861.6:p.Thr357Ser
ENST00000378323.8:c.1196C>G	ENSP00000367574.4:p.Thr399Ser
ENST00000378324.6:c.1025C>G	ENSP00000367575.2:p.Thr342Ser
ENST00000403558.1:c.1310C>G	ENSP00000384420.1:p.Thr437Ser
ENST00000528996.1:c.382C>G	ENSP00000431226.1:n.382C>G
ENST00000530113.1:n.638C>G
ENST00000531133.5:c.682C>G	ENSP00000435431.1:n.682C>G
ENST00000531797.5:c.*206C>G	ENSP00000432554.1:n.*206C>G
ENST00000619430.1:c.349-37C>G	ENSP00000478572.1:n.349-37C>G
NM_000062.2:c.1181C>G , LRG_105t1:c.1181C>G	NP_000053.2:p.Thr394Ser
NM_001032295.1:c.1181C>G	NP_001027466.1:p.Thr394Ser
NM_000062.3:c.1181C>G MANE Select	NP_000053.2:p.Thr394Ser
NM_001032295.2:c.1181C>G	NP_001027466.1:p.Thr394Ser