Canonical Allele Identifier: CA380690952

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382042C>G (hg19) ; chr11:g.57614569C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614569C>G , CM000673.2:g.57614569C>G	GRCh38
NC_000011.9:g.57382042C>G , CM000673.1:g.57382042C>G	GRCh37
NC_000011.8:g.57138618C>G	NCBI36
NG_009625.1:g.22016C>G , LRG_105:g.22016C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1491C>G MANE Select	ENSP00000278407.4:p.Asp497Glu
ENST00000528996.2:c.*388C>G	ENSP00000431226.2:n.*388C>G
ENST00000531605.2:c.*1267C>G	ENSP00000503752.1:n.*1267C>G
ENST00000619430.2:c.1287C>G	ENSP00000478572.2:p.Asp429Glu
ENST00000676670.1:c.1491C>G	ENSP00000504807.1:p.Asp497Glu
ENST00000676741.1:n.2573C>G
ENST00000677624.1:c.*911C>G	ENSP00000503979.1:n.*911C>G
ENST00000677625.1:c.1437C>G	ENSP00000502857.1:p.Asp479Glu
ENST00000677856.1:n.1744C>G
ENST00000677915.1:c.*388C>G	ENSP00000503118.1:n.*388C>G
ENST00000678533.1:c.*1045C>G	ENSP00000503873.1:n.*1045C>G
ENST00000678592.1:c.*431C>G	ENSP00000504424.1:n.*431C>G
ENST00000278407.8:c.1491C>G	ENSP00000278407.4:p.Asp497Glu
ENST00000340687.10:c.1380C>G	ENSP00000341861.6:p.Asp460Glu
ENST00000378323.8:c.1506C>G	ENSP00000367574.4:p.Asp502Glu
ENST00000378324.6:c.1335C>G	ENSP00000367575.2:p.Asp445Glu
ENST00000403558.1:c.1620C>G	ENSP00000384420.1:p.Asp540Glu
ENST00000528996.1:c.692C>G	ENSP00000431226.1:n.692C>G
ENST00000531133.5:c.992C>G	ENSP00000435431.1:n.992C>G
ENST00000531797.5:c.*516C>G	ENSP00000432554.1:n.*516C>G
ENST00000619430.1:c.622C>G	ENSP00000478572.1:n.622C>G
NM_000062.2:c.1491C>G , LRG_105t1:c.1491C>G	NP_000053.2:p.Asp497Glu
NM_001032295.1:c.1491C>G	NP_001027466.1:p.Asp497Glu
NM_000062.3:c.1491C>G MANE Select	NP_000053.2:p.Asp497Glu
NM_001032295.2:c.1491C>G	NP_001027466.1:p.Asp497Glu