Canonical Allele Identifier: CA474806825

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381922T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614449T>G , CM000673.2:g.57614449T>G	GRCh38
NC_000011.9:g.57381922T>G , CM000673.1:g.57381922T>G	GRCh37
NC_000011.8:g.57138498T>G	NCBI36
NG_009625.1:g.21896T>G , LRG_105:g.21896T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1371T>G MANE Select	ENSP00000278407.4:p.Ala457=
ENST00000528996.2:c.*268T>G	ENSP00000431226.2:n.*268T>G
ENST00000531605.2:c.*1147T>G	ENSP00000503752.1:n.*1147T>G
ENST00000619430.2:c.1167T>G	ENSP00000478572.2:p.Ala389=
ENST00000676670.1:c.1371T>G	ENSP00000504807.1:p.Ala457=
ENST00000676741.1:n.2453T>G
ENST00000677624.1:c.*791T>G	ENSP00000503979.1:n.*791T>G
ENST00000677625.1:c.1317T>G	ENSP00000502857.1:p.Ala439=
ENST00000677856.1:n.1624T>G
ENST00000677915.1:c.*268T>G	ENSP00000503118.1:n.*268T>G
ENST00000678533.1:c.*925T>G	ENSP00000503873.1:n.*925T>G
ENST00000678592.1:c.*311T>G	ENSP00000504424.1:n.*311T>G
ENST00000278407.8:c.1371T>G	ENSP00000278407.4:p.Ala457=
ENST00000340687.10:c.1260T>G	ENSP00000341861.6:p.Ala420=
ENST00000378323.8:c.1386T>G	ENSP00000367574.4:p.Ala462=
ENST00000378324.6:c.1215T>G	ENSP00000367575.2:p.Ala405=
ENST00000403558.1:c.1500T>G	ENSP00000384420.1:p.Ala500=
ENST00000528996.1:c.572T>G	ENSP00000431226.1:n.572T>G
ENST00000530113.1:n.828T>G
ENST00000531133.5:c.872T>G	ENSP00000435431.1:n.872T>G
ENST00000531797.5:c.*396T>G	ENSP00000432554.1:n.*396T>G
ENST00000619430.1:c.502T>G	ENSP00000478572.1:n.502T>G
NM_000062.2:c.1371T>G , LRG_105t1:c.1371T>G	NP_000053.2:p.Ala457=
NM_001032295.1:c.1371T>G	NP_001027466.1:p.Ala457=
NM_000062.3:c.1371T>G MANE Select	NP_000053.2:p.Ala457=
NM_001032295.2:c.1371T>G	NP_001027466.1:p.Ala457=