Canonical Allele Identifier: CA380699815

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373683A>T (hg19) ; chr11:g.57606210A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606210A>T , CM000673.2:g.57606210A>T	GRCh38
NC_000011.9:g.57373683A>T , CM000673.1:g.57373683A>T	GRCh37
NC_000011.8:g.57130259A>T	NCBI36
NG_009625.1:g.13657A>T , LRG_105:g.13657A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.886A>T MANE Select	ENSP00000278407.4:p.Ser296Cys
ENST00000528996.2:c.59-5516A>T	ENSP00000431226.2:n.59-5516A>T
ENST00000531605.2:c.*662A>T	ENSP00000503752.1:n.*662A>T
ENST00000619430.2:c.686-198A>T	ENSP00000478572.2:n.686-198A>T
ENST00000676670.1:c.886A>T	ENSP00000504807.1:p.Ser296Cys
ENST00000676741.1:n.1968A>T
ENST00000677624.1:c.*306A>T	ENSP00000503979.1:n.*306A>T
ENST00000677625.1:c.886A>T	ENSP00000502857.1:p.Ser296Cys
ENST00000677856.1:n.945A>T
ENST00000677915.1:c.685+4041A>T	ENSP00000503118.1:n.685+4041A>T
ENST00000678533.1:c.*440A>T	ENSP00000503873.1:n.*440A>T
ENST00000678592.1:c.886A>T	ENSP00000504424.1:p.Ser296Cys
ENST00000278407.8:c.886A>T	ENSP00000278407.4:p.Ser296Cys
ENST00000340687.10:c.886A>T	ENSP00000341861.6:p.Ser296Cys
ENST00000378323.8:c.901A>T	ENSP00000367574.4:p.Ser301Cys
ENST00000378324.6:c.730A>T	ENSP00000367575.2:p.Ser244Cys
ENST00000403558.1:c.988A>T	ENSP00000384420.1:p.Ser330Cys
ENST00000531133.5:c.387A>T	ENSP00000435431.1:n.387A>T
ENST00000531797.5:c.*54+4041A>T	ENSP00000432554.1:n.*54+4041A>T
ENST00000619430.1:c.349-5695A>T	ENSP00000478572.1:n.349-5695A>T
NM_000062.2:c.886A>T , LRG_105t1:c.886A>T	NP_000053.2:p.Ser296Cys
NM_001032295.1:c.886A>T	NP_001027466.1:p.Ser296Cys
NM_000062.3:c.886A>T MANE Select	NP_000053.2:p.Ser296Cys
NM_001032295.2:c.886A>T	NP_001027466.1:p.Ser296Cys