Canonical Allele Identifier: CA474806809

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57381913G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614440G>T , CM000673.2:g.57614440G>T	GRCh38
NC_000011.9:g.57381913G>T , CM000673.1:g.57381913G>T	GRCh37
NC_000011.8:g.57138489G>T	NCBI36
NG_009625.1:g.21887G>T , LRG_105:g.21887G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1362G>T MANE Select	ENSP00000278407.4:p.Val454=
ENST00000528996.2:c.*259G>T	ENSP00000431226.2:n.*259G>T
ENST00000531605.2:c.*1138G>T	ENSP00000503752.1:n.*1138G>T
ENST00000619430.2:c.1158G>T	ENSP00000478572.2:p.Val386=
ENST00000676670.1:c.1362G>T	ENSP00000504807.1:p.Val454=
ENST00000676741.1:n.2444G>T
ENST00000677624.1:c.*782G>T	ENSP00000503979.1:n.*782G>T
ENST00000677625.1:c.1308G>T	ENSP00000502857.1:p.Val436=
ENST00000677856.1:n.1615G>T
ENST00000677915.1:c.*259G>T	ENSP00000503118.1:n.*259G>T
ENST00000678533.1:c.*916G>T	ENSP00000503873.1:n.*916G>T
ENST00000678592.1:c.*302G>T	ENSP00000504424.1:n.*302G>T
ENST00000278407.8:c.1362G>T	ENSP00000278407.4:p.Val454=
ENST00000340687.10:c.1251G>T	ENSP00000341861.6:p.Val417=
ENST00000378323.8:c.1377G>T	ENSP00000367574.4:p.Val459=
ENST00000378324.6:c.1206G>T	ENSP00000367575.2:p.Val402=
ENST00000403558.1:c.1491G>T	ENSP00000384420.1:p.Val497=
ENST00000528996.1:c.563G>T	ENSP00000431226.1:n.563G>T
ENST00000530113.1:n.819G>T
ENST00000531133.5:c.863G>T	ENSP00000435431.1:n.863G>T
ENST00000531797.5:c.*387G>T	ENSP00000432554.1:n.*387G>T
ENST00000619430.1:c.493G>T	ENSP00000478572.1:n.493G>T
NM_000062.2:c.1362G>T , LRG_105t1:c.1362G>T	NP_000053.2:p.Val454=
NM_001032295.1:c.1362G>T	NP_001027466.1:p.Val454=
NM_000062.3:c.1362G>T MANE Select	NP_000053.2:p.Val454=
NM_001032295.2:c.1362G>T	NP_001027466.1:p.Val454=