Canonical Allele Identifier: CA474567637

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379232C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611759C>T , CM000673.2:g.57611759C>T	GRCh38
NC_000011.9:g.57379232C>T , CM000673.1:g.57379232C>T	GRCh37
NC_000011.8:g.57135808C>T	NCBI36
NG_009625.1:g.19206C>T , LRG_105:g.19206C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1072C>T MANE Select	ENSP00000278407.4:p.Leu358=
ENST00000528996.2:c.92C>T	ENSP00000431226.2:p.Pro31Leu
ENST00000531605.2:c.*848C>T	ENSP00000503752.1:n.*848C>T
ENST00000619430.2:c.868C>T	ENSP00000478572.2:p.Leu290=
ENST00000676670.1:c.1072C>T	ENSP00000504807.1:p.Leu358=
ENST00000676741.1:n.2154C>T
ENST00000677624.1:c.*492C>T	ENSP00000503979.1:n.*492C>T
ENST00000677625.1:c.1030-12C>T	ENSP00000502857.1:n.1030-12C>T
ENST00000677856.1:n.1325C>T
ENST00000677915.1:c.728C>T	ENSP00000503118.1:p.Pro243Leu
ENST00000678533.1:c.*626C>T	ENSP00000503873.1:n.*626C>T
ENST00000678592.1:c.*12C>T	ENSP00000504424.1:n.*12C>T
ENST00000278407.8:c.1072C>T	ENSP00000278407.4:p.Leu358=
ENST00000340687.10:c.1030-69C>T	ENSP00000341861.6:n.1030-69C>T
ENST00000378323.8:c.1087C>T	ENSP00000367574.4:p.Leu363=
ENST00000378324.6:c.916C>T	ENSP00000367575.2:p.Leu306=
ENST00000403558.1:c.1201C>T	ENSP00000384420.1:p.Leu401=
ENST00000528996.1:c.273C>T	ENSP00000431226.1:n.273C>T
ENST00000530113.1:n.529C>T
ENST00000531133.5:c.573C>T	ENSP00000435431.1:n.573C>T
ENST00000531797.5:c.*97C>T	ENSP00000432554.1:n.*97C>T
ENST00000619430.1:c.349-146C>T	ENSP00000478572.1:n.349-146C>T
NM_000062.2:c.1072C>T , LRG_105t1:c.1072C>T	NP_000053.2:p.Leu358=
NM_001032295.1:c.1072C>T	NP_001027466.1:p.Leu358=
NM_000062.3:c.1072C>T MANE Select	NP_000053.2:p.Leu358=
NM_001032295.2:c.1072C>T	NP_001027466.1:p.Leu358=