Canonical Allele Identifier: CA474806913

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381970G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614497G>T , CM000673.2:g.57614497G>T	GRCh38
NC_000011.9:g.57381970G>T , CM000673.1:g.57381970G>T	GRCh37
NC_000011.8:g.57138546G>T	NCBI36
NG_009625.1:g.21944G>T , LRG_105:g.21944G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1419G>T MANE Select	ENSP00000278407.4:p.Val473=
ENST00000528996.2:c.*316G>T	ENSP00000431226.2:n.*316G>T
ENST00000531605.2:c.*1195G>T	ENSP00000503752.1:n.*1195G>T
ENST00000619430.2:c.1215G>T	ENSP00000478572.2:p.Val405=
ENST00000676670.1:c.1419G>T	ENSP00000504807.1:p.Val473=
ENST00000676741.1:n.2501G>T
ENST00000677624.1:c.*839G>T	ENSP00000503979.1:n.*839G>T
ENST00000677625.1:c.1365G>T	ENSP00000502857.1:p.Val455=
ENST00000677856.1:n.1672G>T
ENST00000677915.1:c.*316G>T	ENSP00000503118.1:n.*316G>T
ENST00000678533.1:c.*973G>T	ENSP00000503873.1:n.*973G>T
ENST00000678592.1:c.*359G>T	ENSP00000504424.1:n.*359G>T
ENST00000278407.8:c.1419G>T	ENSP00000278407.4:p.Val473=
ENST00000340687.10:c.1308G>T	ENSP00000341861.6:p.Val436=
ENST00000378323.8:c.1434G>T	ENSP00000367574.4:p.Val478=
ENST00000378324.6:c.1263G>T	ENSP00000367575.2:p.Val421=
ENST00000403558.1:c.1548G>T	ENSP00000384420.1:p.Val516=
ENST00000528996.1:c.620G>T	ENSP00000431226.1:n.620G>T
ENST00000530113.1:n.876G>T
ENST00000531133.5:c.920G>T	ENSP00000435431.1:n.920G>T
ENST00000531797.5:c.*444G>T	ENSP00000432554.1:n.*444G>T
ENST00000619430.1:c.550G>T	ENSP00000478572.1:n.550G>T
NM_000062.2:c.1419G>T , LRG_105t1:c.1419G>T	NP_000053.2:p.Val473=
NM_001032295.1:c.1419G>T	NP_001027466.1:p.Val473=
NM_000062.3:c.1419G>T MANE Select	NP_000053.2:p.Val473=
NM_001032295.2:c.1419G>T	NP_001027466.1:p.Val473=