Canonical Allele Identifier: CA2613603470

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614622-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614622C>A , CM000673.2:g.57614622C>A	GRCh38
NC_000011.9:g.57382095C>A , CM000673.1:g.57382095C>A	GRCh37
NC_000011.8:g.57138671C>A	NCBI36
NG_009625.1:g.22069C>A , LRG_105:g.22069C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.*41C>A MANE Select	ENSP00000278407.4:n.*41C>A
ENST00000528996.2:c.*441C>A	ENSP00000431226.2:n.*441C>A
ENST00000531605.2:c.*1320C>A	ENSP00000503752.1:n.*1320C>A
ENST00000619430.2:c.*41C>A	ENSP00000478572.2:n.*41C>A
ENST00000676670.1:c.*15+26C>A	ENSP00000504807.1:n.*15+26C>A
ENST00000676741.1:n.2626C>A
ENST00000677624.1:c.*964C>A	ENSP00000503979.1:n.*964C>A
ENST00000677625.1:c.*41C>A	ENSP00000502857.1:n.*41C>A
ENST00000677856.1:n.1797C>A
ENST00000677915.1:c.*441C>A	ENSP00000503118.1:n.*441C>A
ENST00000678533.1:c.*1072+26C>A	ENSP00000503873.1:n.*1072+26C>A
ENST00000678592.1:c.*484C>A	ENSP00000504424.1:n.*484C>A
ENST00000278407.8:c.*41C>A	ENSP00000278407.4:n.*41C>A
ENST00000340687.10:c.*41C>A	ENSP00000341861.6:n.*41C>A
ENST00000378323.8:c.*41C>A	ENSP00000367574.4:n.*41C>A
ENST00000378324.6:c.*41C>A	ENSP00000367575.2:n.*41C>A
ENST00000403558.1:c.*41C>A	ENSP00000384420.1:n.*41C>A
ENST00000528996.1:c.745C>A	ENSP00000431226.1:n.745C>A
ENST00000531797.5:c.*569C>A	ENSP00000432554.1:n.*569C>A
NM_000062.2:c.*41C>A , LRG_105t1:c.*41C>A	NP_000053.2:n.*41C>A
NM_001032295.1:c.*41C>A	NP_001027466.1:n.*41C>A
NM_000062.3:c.*41C>A MANE Select	NP_000053.2:n.*41C>A
NM_001032295.2:c.*41C>A	NP_001027466.1:n.*41C>A