Canonical Allele Identifier: CA2613603550

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614641-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614641C>T , CM000673.2:g.57614641C>T	GRCh38
NC_000011.9:g.57382114C>T , CM000673.1:g.57382114C>T	GRCh37
NC_000011.8:g.57138690C>T	NCBI36
NG_009625.1:g.22088C>T , LRG_105:g.22088C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*60C>T MANE Select	ENSP00000278407.4:n.*60C>T
ENST00000528996.2:c.*460C>T	ENSP00000431226.2:n.*460C>T
ENST00000531605.2:c.*1339C>T	ENSP00000503752.1:n.*1339C>T
ENST00000619430.2:c.*60C>T	ENSP00000478572.2:n.*60C>T
ENST00000676670.1:c.*15+45C>T	ENSP00000504807.1:n.*15+45C>T
ENST00000676741.1:n.2645C>T
ENST00000677624.1:c.*983C>T	ENSP00000503979.1:n.*983C>T
ENST00000677625.1:c.*60C>T	ENSP00000502857.1:n.*60C>T
ENST00000677856.1:n.1816C>T
ENST00000677915.1:c.*460C>T	ENSP00000503118.1:n.*460C>T
ENST00000678533.1:c.*1072+45C>T	ENSP00000503873.1:n.*1072+45C>T
ENST00000678592.1:c.*503C>T	ENSP00000504424.1:n.*503C>T
ENST00000278407.8:c.*60C>T	ENSP00000278407.4:n.*60C>T
ENST00000340687.10:c.*60C>T	ENSP00000341861.6:n.*60C>T
ENST00000378323.8:c.*60C>T	ENSP00000367574.4:n.*60C>T
ENST00000378324.6:c.*60C>T	ENSP00000367575.2:n.*60C>T
ENST00000403558.1:c.*60C>T	ENSP00000384420.1:n.*60C>T
ENST00000528996.1:c.764C>T	ENSP00000431226.1:n.764C>T
ENST00000531797.5:c.*588C>T	ENSP00000432554.1:n.*588C>T
NM_000062.2:c.*60C>T , LRG_105t1:c.*60C>T	NP_000053.2:n.*60C>T
NM_001032295.1:c.*60C>T	NP_001027466.1:n.*60C>T
NM_000062.3:c.*60C>T MANE Select	NP_000053.2:n.*60C>T
NM_001032295.2:c.*60C>T	NP_001027466.1:n.*60C>T