Canonical Allele Identifier: CA380703454

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379382G>T (hg19) ; chr11:g.57611909G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611909G>T , CM000673.2:g.57611909G>T	GRCh38
NC_000011.9:g.57379382G>T , CM000673.1:g.57379382G>T	GRCh37
NC_000011.8:g.57135958G>T	NCBI36
NG_009625.1:g.19356G>T , LRG_105:g.19356G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1222G>T MANE Select	ENSP00000278407.4:p.Asp408Tyr
ENST00000528996.2:c.*119G>T	ENSP00000431226.2:n.*119G>T
ENST00000531605.2:c.*998G>T	ENSP00000503752.1:n.*998G>T
ENST00000619430.2:c.1018G>T	ENSP00000478572.2:p.Asp340Tyr
ENST00000676670.1:c.1222G>T	ENSP00000504807.1:p.Asp408Tyr
ENST00000676741.1:n.2304G>T
ENST00000677624.1:c.*642G>T	ENSP00000503979.1:n.*642G>T
ENST00000677625.1:c.1168G>T	ENSP00000502857.1:p.Asp390Tyr
ENST00000677856.1:n.1475G>T
ENST00000677915.1:c.*119G>T	ENSP00000503118.1:n.*119G>T
ENST00000678533.1:c.*776G>T	ENSP00000503873.1:n.*776G>T
ENST00000678592.1:c.*162G>T	ENSP00000504424.1:n.*162G>T
ENST00000278407.8:c.1222G>T	ENSP00000278407.4:p.Asp408Tyr
ENST00000340687.10:c.1111G>T	ENSP00000341861.6:p.Asp371Tyr
ENST00000378323.8:c.1237G>T	ENSP00000367574.4:p.Asp413Tyr
ENST00000378324.6:c.1066G>T	ENSP00000367575.2:p.Asp356Tyr
ENST00000403558.1:c.1351G>T	ENSP00000384420.1:p.Asp451Tyr
ENST00000528996.1:c.423G>T	ENSP00000431226.1:n.423G>T
ENST00000530113.1:n.679G>T
ENST00000531133.5:c.723G>T	ENSP00000435431.1:n.723G>T
ENST00000531797.5:c.*247G>T	ENSP00000432554.1:n.*247G>T
ENST00000619430.1:c.353G>T	ENSP00000478572.1:p.Gly118Val
NM_000062.2:c.1222G>T , LRG_105t1:c.1222G>T	NP_000053.2:p.Asp408Tyr
NM_001032295.1:c.1222G>T	NP_001027466.1:p.Asp408Tyr
NM_000062.3:c.1222G>T MANE Select	NP_000053.2:p.Asp408Tyr
NM_001032295.2:c.1222G>T	NP_001027466.1:p.Asp408Tyr