Canonical Allele Identifier: CA380690771

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381964T>G (hg19) ; chr11:g.57614491T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614491T>G , CM000673.2:g.57614491T>G	GRCh38
NC_000011.9:g.57381964T>G , CM000673.1:g.57381964T>G	GRCh37
NC_000011.8:g.57138540T>G	NCBI36
NG_009625.1:g.21938T>G , LRG_105:g.21938T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1413T>G MANE Select	ENSP00000278407.4:p.Phe471Leu
ENST00000528996.2:c.*310T>G	ENSP00000431226.2:n.*310T>G
ENST00000531605.2:c.*1189T>G	ENSP00000503752.1:n.*1189T>G
ENST00000619430.2:c.1209T>G	ENSP00000478572.2:p.Phe403Leu
ENST00000676670.1:c.1413T>G	ENSP00000504807.1:p.Phe471Leu
ENST00000676741.1:n.2495T>G
ENST00000677624.1:c.*833T>G	ENSP00000503979.1:n.*833T>G
ENST00000677625.1:c.1359T>G	ENSP00000502857.1:p.Phe453Leu
ENST00000677856.1:n.1666T>G
ENST00000677915.1:c.*310T>G	ENSP00000503118.1:n.*310T>G
ENST00000678533.1:c.*967T>G	ENSP00000503873.1:n.*967T>G
ENST00000678592.1:c.*353T>G	ENSP00000504424.1:n.*353T>G
ENST00000278407.8:c.1413T>G	ENSP00000278407.4:p.Phe471Leu
ENST00000340687.10:c.1302T>G	ENSP00000341861.6:p.Phe434Leu
ENST00000378323.8:c.1428T>G	ENSP00000367574.4:p.Phe476Leu
ENST00000378324.6:c.1257T>G	ENSP00000367575.2:p.Phe419Leu
ENST00000403558.1:c.1542T>G	ENSP00000384420.1:p.Phe514Leu
ENST00000528996.1:c.614T>G	ENSP00000431226.1:n.614T>G
ENST00000530113.1:n.870T>G
ENST00000531133.5:c.914T>G	ENSP00000435431.1:n.914T>G
ENST00000531797.5:c.*438T>G	ENSP00000432554.1:n.*438T>G
ENST00000619430.1:c.544T>G	ENSP00000478572.1:n.544T>G
NM_000062.2:c.1413T>G , LRG_105t1:c.1413T>G	NP_000053.2:p.Phe471Leu
NM_001032295.1:c.1413T>G	NP_001027466.1:p.Phe471Leu
NM_000062.3:c.1413T>G MANE Select	NP_000053.2:p.Phe471Leu
NM_001032295.2:c.1413T>G	NP_001027466.1:p.Phe471Leu