Canonical Allele Identifier: CA380699805

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57373681T>G (hg19) ; chr11:g.57606208T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57606208T>G , CM000673.2:g.57606208T>G	GRCh38
NC_000011.9:g.57373681T>G , CM000673.1:g.57373681T>G	GRCh37
NC_000011.8:g.57130257T>G	NCBI36
NG_009625.1:g.13655T>G , LRG_105:g.13655T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.884T>G MANE Select	ENSP00000278407.4:p.Leu295Arg
ENST00000528996.2:c.59-5518T>G	ENSP00000431226.2:n.59-5518T>G
ENST00000531605.2:c.*660T>G	ENSP00000503752.1:n.*660T>G
ENST00000619430.2:c.686-200T>G	ENSP00000478572.2:n.686-200T>G
ENST00000676670.1:c.884T>G	ENSP00000504807.1:p.Leu295Arg
ENST00000676741.1:n.1966T>G
ENST00000677624.1:c.*304T>G	ENSP00000503979.1:n.*304T>G
ENST00000677625.1:c.884T>G	ENSP00000502857.1:p.Leu295Arg
ENST00000677856.1:n.943T>G
ENST00000677915.1:c.685+4039T>G	ENSP00000503118.1:n.685+4039T>G
ENST00000678533.1:c.*438T>G	ENSP00000503873.1:n.*438T>G
ENST00000678592.1:c.884T>G	ENSP00000504424.1:p.Leu295Arg
ENST00000278407.8:c.884T>G	ENSP00000278407.4:p.Leu295Arg
ENST00000340687.10:c.884T>G	ENSP00000341861.6:p.Leu295Arg
ENST00000378323.8:c.899T>G	ENSP00000367574.4:p.Leu300Arg
ENST00000378324.6:c.728T>G	ENSP00000367575.2:p.Leu243Arg
ENST00000403558.1:c.986T>G	ENSP00000384420.1:p.Leu329Arg
ENST00000531133.5:c.385T>G	ENSP00000435431.1:n.385T>G
ENST00000531797.5:c.*54+4039T>G	ENSP00000432554.1:n.*54+4039T>G
ENST00000619430.1:c.349-5697T>G	ENSP00000478572.1:n.349-5697T>G
NM_000062.2:c.884T>G , LRG_105t1:c.884T>G	NP_000053.2:p.Leu295Arg
NM_001032295.1:c.884T>G	NP_001027466.1:p.Leu295Arg
NM_000062.3:c.884T>G MANE Select	NP_000053.2:p.Leu295Arg
NM_001032295.2:c.884T>G	NP_001027466.1:p.Leu295Arg