Canonical Allele Identifier: CA380703374

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379363C>G (hg19) ; chr11:g.57611890C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611890C>G , CM000673.2:g.57611890C>G	GRCh38
NC_000011.9:g.57379363C>G , CM000673.1:g.57379363C>G	GRCh37
NC_000011.8:g.57135939C>G	NCBI36
NG_009625.1:g.19337C>G , LRG_105:g.19337C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1203C>G MANE Select	ENSP00000278407.4:p.Ile401Met
ENST00000528996.2:c.*100C>G	ENSP00000431226.2:n.*100C>G
ENST00000531605.2:c.*979C>G	ENSP00000503752.1:n.*979C>G
ENST00000619430.2:c.999C>G	ENSP00000478572.2:p.Ile333Met
ENST00000676670.1:c.1203C>G	ENSP00000504807.1:p.Ile401Met
ENST00000676741.1:n.2285C>G
ENST00000677624.1:c.*623C>G	ENSP00000503979.1:n.*623C>G
ENST00000677625.1:c.1149C>G	ENSP00000502857.1:p.Ile383Met
ENST00000677856.1:n.1456C>G
ENST00000677915.1:c.*100C>G	ENSP00000503118.1:n.*100C>G
ENST00000678533.1:c.*757C>G	ENSP00000503873.1:n.*757C>G
ENST00000678592.1:c.*143C>G	ENSP00000504424.1:n.*143C>G
ENST00000278407.8:c.1203C>G	ENSP00000278407.4:p.Ile401Met
ENST00000340687.10:c.1092C>G	ENSP00000341861.6:p.Ile364Met
ENST00000378323.8:c.1218C>G	ENSP00000367574.4:p.Ile406Met
ENST00000378324.6:c.1047C>G	ENSP00000367575.2:p.Ile349Met
ENST00000403558.1:c.1332C>G	ENSP00000384420.1:p.Ile444Met
ENST00000528996.1:c.404C>G	ENSP00000431226.1:n.404C>G
ENST00000530113.1:n.660C>G
ENST00000531133.5:c.704C>G	ENSP00000435431.1:n.704C>G
ENST00000531797.5:c.*228C>G	ENSP00000432554.1:n.*228C>G
ENST00000619430.1:c.349-15C>G	ENSP00000478572.1:n.349-15C>G
NM_000062.2:c.1203C>G , LRG_105t1:c.1203C>G	NP_000053.2:p.Ile401Met
NM_001032295.1:c.1203C>G	NP_001027466.1:p.Ile401Met
NM_000062.3:c.1203C>G MANE Select	NP_000053.2:p.Ile401Met
NM_001032295.2:c.1203C>G	NP_001027466.1:p.Ile401Met