Canonical Allele Identifier: CA380690904

Gene: SERPING1

Linked Data

• MyVariant Identifiers: chr11:g.57382019G>T (hg19) ; chr11:g.57614546G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614546G>T , CM000673.2:g.57614546G>T	GRCh38
NC_000011.9:g.57382019G>T , CM000673.1:g.57382019G>T	GRCh37
NC_000011.8:g.57138595G>T	NCBI36
NG_009625.1:g.21993G>T , LRG_105:g.21993G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1468G>T MANE Select	ENSP00000278407.4:p.Val490Phe
ENST00000528996.2:c.*365G>T	ENSP00000431226.2:n.*365G>T
ENST00000531605.2:c.*1244G>T	ENSP00000503752.1:n.*1244G>T
ENST00000619430.2:c.1264G>T	ENSP00000478572.2:p.Val422Phe
ENST00000676670.1:c.1468G>T	ENSP00000504807.1:p.Val490Phe
ENST00000676741.1:n.2550G>T
ENST00000677624.1:c.*888G>T	ENSP00000503979.1:n.*888G>T
ENST00000677625.1:c.1414G>T	ENSP00000502857.1:p.Val472Phe
ENST00000677856.1:n.1721G>T
ENST00000677915.1:c.*365G>T	ENSP00000503118.1:n.*365G>T
ENST00000678533.1:c.*1022G>T	ENSP00000503873.1:n.*1022G>T
ENST00000678592.1:c.*408G>T	ENSP00000504424.1:n.*408G>T
ENST00000278407.8:c.1468G>T	ENSP00000278407.4:p.Val490Phe
ENST00000340687.10:c.1357G>T	ENSP00000341861.6:p.Val453Phe
ENST00000378323.8:c.1483G>T	ENSP00000367574.4:p.Val495Phe
ENST00000378324.6:c.1312G>T	ENSP00000367575.2:p.Val438Phe
ENST00000403558.1:c.1597G>T	ENSP00000384420.1:p.Val533Phe
ENST00000528996.1:c.669G>T	ENSP00000431226.1:n.669G>T
ENST00000531133.5:c.969G>T	ENSP00000435431.1:n.969G>T
ENST00000531797.5:c.*493G>T	ENSP00000432554.1:n.*493G>T
ENST00000619430.1:c.599G>T	ENSP00000478572.1:n.599G>T
NM_000062.2:c.1468G>T , LRG_105t1:c.1468G>T	NP_000053.2:p.Val490Phe
NM_001032295.1:c.1468G>T	NP_001027466.1:p.Val490Phe
NM_000062.3:c.1468G>T MANE Select	NP_000053.2:p.Val490Phe
NM_001032295.2:c.1468G>T	NP_001027466.1:p.Val490Phe