Canonical Allele Identifier: CA474568234

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379327C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611854C>G , CM000673.2:g.57611854C>G	GRCh38
NC_000011.9:g.57379327C>G , CM000673.1:g.57379327C>G	GRCh37
NC_000011.8:g.57135903C>G	NCBI36
NG_009625.1:g.19301C>G , LRG_105:g.19301C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1167C>G MANE Select	ENSP00000278407.4:p.Ser389=
ENST00000528996.2:c.*64C>G	ENSP00000431226.2:n.*64C>G
ENST00000531605.2:c.*943C>G	ENSP00000503752.1:n.*943C>G
ENST00000619430.2:c.963C>G	ENSP00000478572.2:p.Ser321=
ENST00000676670.1:c.1167C>G	ENSP00000504807.1:p.Ser389=
ENST00000676741.1:n.2249C>G
ENST00000677624.1:c.*587C>G	ENSP00000503979.1:n.*587C>G
ENST00000677625.1:c.1113C>G	ENSP00000502857.1:p.Ser371=
ENST00000677856.1:n.1420C>G
ENST00000677915.1:c.*64C>G	ENSP00000503118.1:n.*64C>G
ENST00000678533.1:c.*721C>G	ENSP00000503873.1:n.*721C>G
ENST00000678592.1:c.*107C>G	ENSP00000504424.1:n.*107C>G
ENST00000278407.8:c.1167C>G	ENSP00000278407.4:p.Ser389=
ENST00000340687.10:c.1056C>G	ENSP00000341861.6:p.Ser352=
ENST00000378323.8:c.1182C>G	ENSP00000367574.4:p.Ser394=
ENST00000378324.6:c.1011C>G	ENSP00000367575.2:p.Ser337=
ENST00000403558.1:c.1296C>G	ENSP00000384420.1:p.Ser432=
ENST00000528996.1:c.368C>G	ENSP00000431226.1:n.368C>G
ENST00000530113.1:n.624C>G
ENST00000531133.5:c.668C>G	ENSP00000435431.1:n.668C>G
ENST00000531797.5:c.*192C>G	ENSP00000432554.1:n.*192C>G
ENST00000619430.1:c.349-51C>G	ENSP00000478572.1:n.349-51C>G
NM_000062.2:c.1167C>G , LRG_105t1:c.1167C>G	NP_000053.2:p.Ser389=
NM_001032295.1:c.1167C>G	NP_001027466.1:p.Ser389=
NM_000062.3:c.1167C>G MANE Select	NP_000053.2:p.Ser389=
NM_001032295.2:c.1167C>G	NP_001027466.1:p.Ser389=