Canonical Allele Identifier: CA380702707

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379260T>C (hg19) ; chr11:g.57611787T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611787T>C , CM000673.2:g.57611787T>C	GRCh38
NC_000011.9:g.57379260T>C , CM000673.1:g.57379260T>C	GRCh37
NC_000011.8:g.57135836T>C	NCBI36
NG_009625.1:g.19234T>C , LRG_105:g.19234T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1100T>C MANE Select	ENSP00000278407.4:p.Leu367Pro
ENST00000528996.2:c.120T>C	ENSP00000431226.2:p.Ser40=
ENST00000531605.2:c.*876T>C	ENSP00000503752.1:n.*876T>C
ENST00000619430.2:c.896T>C	ENSP00000478572.2:p.Leu299Pro
ENST00000676670.1:c.1100T>C	ENSP00000504807.1:p.Leu367Pro
ENST00000676741.1:n.2182T>C
ENST00000677624.1:c.*520T>C	ENSP00000503979.1:n.*520T>C
ENST00000677625.1:c.1046T>C	ENSP00000502857.1:p.Leu349Pro
ENST00000677856.1:n.1353T>C
ENST00000677915.1:c.756T>C	ENSP00000503118.1:p.Ser252=
ENST00000678533.1:c.*654T>C	ENSP00000503873.1:n.*654T>C
ENST00000678592.1:c.*40T>C	ENSP00000504424.1:n.*40T>C
ENST00000278407.8:c.1100T>C	ENSP00000278407.4:p.Leu367Pro
ENST00000340687.10:c.1030-41T>C	ENSP00000341861.6:n.1030-41T>C
ENST00000378323.8:c.1115T>C	ENSP00000367574.4:p.Leu372Pro
ENST00000378324.6:c.944T>C	ENSP00000367575.2:p.Leu315Pro
ENST00000403558.1:c.1229T>C	ENSP00000384420.1:p.Leu410Pro
ENST00000528996.1:c.301T>C	ENSP00000431226.1:n.301T>C
ENST00000530113.1:n.557T>C
ENST00000531133.5:c.601T>C	ENSP00000435431.1:n.601T>C
ENST00000531797.5:c.*125T>C	ENSP00000432554.1:n.*125T>C
ENST00000619430.1:c.349-118T>C	ENSP00000478572.1:n.349-118T>C
NM_000062.2:c.1100T>C , LRG_105t1:c.1100T>C	NP_000053.2:p.Leu367Pro
NM_001032295.1:c.1100T>C	NP_001027466.1:p.Leu367Pro
NM_000062.3:c.1100T>C MANE Select	NP_000053.2:p.Leu367Pro
NM_001032295.2:c.1100T>C	NP_001027466.1:p.Leu367Pro