Canonical Allele Identifier: CA474567985

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57379288T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57611815T>A , CM000673.2:g.57611815T>A	GRCh38
NC_000011.9:g.57379288T>A , CM000673.1:g.57379288T>A	GRCh37
NC_000011.8:g.57135864T>A	NCBI36
NG_009625.1:g.19262T>A , LRG_105:g.19262T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1128T>A MANE Select	ENSP00000278407.4:p.Pro376=
ENST00000528996.2:c.*25T>A	ENSP00000431226.2:n.*25T>A
ENST00000531605.2:c.*904T>A	ENSP00000503752.1:n.*904T>A
ENST00000619430.2:c.924T>A	ENSP00000478572.2:p.Pro308=
ENST00000676670.1:c.1128T>A	ENSP00000504807.1:p.Pro376=
ENST00000676741.1:n.2210T>A
ENST00000677624.1:c.*548T>A	ENSP00000503979.1:n.*548T>A
ENST00000677625.1:c.1074T>A	ENSP00000502857.1:p.Pro358=
ENST00000677856.1:n.1381T>A
ENST00000677915.1:c.*25T>A	ENSP00000503118.1:n.*25T>A
ENST00000678533.1:c.*682T>A	ENSP00000503873.1:n.*682T>A
ENST00000678592.1:c.*68T>A	ENSP00000504424.1:n.*68T>A
ENST00000278407.8:c.1128T>A	ENSP00000278407.4:p.Pro376=
ENST00000340687.10:c.1030-13T>A	ENSP00000341861.6:n.1030-13T>A
ENST00000378323.8:c.1143T>A	ENSP00000367574.4:p.Pro381=
ENST00000378324.6:c.972T>A	ENSP00000367575.2:p.Pro324=
ENST00000403558.1:c.1257T>A	ENSP00000384420.1:p.Pro419=
ENST00000528996.1:c.329T>A	ENSP00000431226.1:n.329T>A
ENST00000530113.1:n.585T>A
ENST00000531133.5:c.629T>A	ENSP00000435431.1:n.629T>A
ENST00000531797.5:c.*153T>A	ENSP00000432554.1:n.*153T>A
ENST00000619430.1:c.349-90T>A	ENSP00000478572.1:n.349-90T>A
NM_000062.2:c.1128T>A , LRG_105t1:c.1128T>A	NP_000053.2:p.Pro376=
NM_001032295.1:c.1128T>A	NP_001027466.1:p.Pro376=
NM_000062.3:c.1128T>A MANE Select	NP_000053.2:p.Pro376=
NM_001032295.2:c.1128T>A	NP_001027466.1:p.Pro376=