Canonical Allele Identifier: CA474806739

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381850C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614377C>T , CM000673.2:g.57614377C>T	GRCh38
NC_000011.9:g.57381850C>T , CM000673.1:g.57381850C>T	GRCh37
NC_000011.8:g.57138426C>T	NCBI36
NG_009625.1:g.21824C>T , LRG_105:g.21824C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1299C>T MANE Select	ENSP00000278407.4:p.Asp433=
ENST00000528996.2:c.*196C>T	ENSP00000431226.2:n.*196C>T
ENST00000531605.2:c.*1075C>T	ENSP00000503752.1:n.*1075C>T
ENST00000619430.2:c.1095C>T	ENSP00000478572.2:p.Asp365=
ENST00000676670.1:c.1299C>T	ENSP00000504807.1:p.Asp433=
ENST00000676741.1:n.2381C>T
ENST00000677624.1:c.*719C>T	ENSP00000503979.1:n.*719C>T
ENST00000677625.1:c.1245C>T	ENSP00000502857.1:p.Asp415=
ENST00000677856.1:n.1552C>T
ENST00000677915.1:c.*196C>T	ENSP00000503118.1:n.*196C>T
ENST00000678533.1:c.*853C>T	ENSP00000503873.1:n.*853C>T
ENST00000678592.1:c.*239C>T	ENSP00000504424.1:n.*239C>T
ENST00000278407.8:c.1299C>T	ENSP00000278407.4:p.Asp433=
ENST00000340687.10:c.1188C>T	ENSP00000341861.6:p.Asp396=
ENST00000378323.8:c.1314C>T	ENSP00000367574.4:p.Asp438=
ENST00000378324.6:c.1143C>T	ENSP00000367575.2:p.Asp381=
ENST00000403558.1:c.1428C>T	ENSP00000384420.1:p.Asp476=
ENST00000528996.1:c.500C>T	ENSP00000431226.1:n.500C>T
ENST00000530113.1:n.756C>T
ENST00000531133.5:c.800C>T	ENSP00000435431.1:n.800C>T
ENST00000531797.5:c.*324C>T	ENSP00000432554.1:n.*324C>T
ENST00000619430.1:c.430C>T	ENSP00000478572.1:n.430C>T
NM_000062.2:c.1299C>T , LRG_105t1:c.1299C>T	NP_000053.2:p.Asp433=
NM_001032295.1:c.1299C>T	NP_001027466.1:p.Asp433=
NM_000062.3:c.1299C>T MANE Select	NP_000053.2:p.Asp433=
NM_001032295.2:c.1299C>T	NP_001027466.1:p.Asp433=