Canonical Allele Identifier: CA2574828297

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614276-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614276C>A , CM000673.2:g.57614276C>A	GRCh38
NC_000011.9:g.57381749C>A , CM000673.1:g.57381749C>A	GRCh37
NC_000011.8:g.57138325C>A	NCBI36
NG_009625.1:g.21723C>A , LRG_105:g.21723C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.1250-52C>A MANE Select	ENSP00000278407.4:n.1250-52C>A
ENST00000528996.2:c.*147-52C>A	ENSP00000431226.2:n.*147-52C>A
ENST00000531605.2:c.*1026-52C>A	ENSP00000503752.1:n.*1026-52C>A
ENST00000619430.2:c.1046-52C>A	ENSP00000478572.2:n.1046-52C>A
ENST00000676670.1:c.1250-52C>A	ENSP00000504807.1:n.1250-52C>A
ENST00000676741.1:n.2332-52C>A
ENST00000677624.1:c.*670-52C>A	ENSP00000503979.1:n.*670-52C>A
ENST00000677625.1:c.1196-52C>A	ENSP00000502857.1:n.1196-52C>A
ENST00000677856.1:n.1503-52C>A
ENST00000677915.1:c.*147-52C>A	ENSP00000503118.1:n.*147-52C>A
ENST00000678533.1:c.*804-52C>A	ENSP00000503873.1:n.*804-52C>A
ENST00000678592.1:c.*190-52C>A	ENSP00000504424.1:n.*190-52C>A
ENST00000278407.8:c.1250-52C>A	ENSP00000278407.4:n.1250-52C>A
ENST00000340687.10:c.1139-52C>A	ENSP00000341861.6:n.1139-52C>A
ENST00000378323.8:c.1265-52C>A	ENSP00000367574.4:n.1265-52C>A
ENST00000378324.6:c.1094-52C>A	ENSP00000367575.2:n.1094-52C>A
ENST00000403558.1:c.1379-52C>A	ENSP00000384420.1:n.1379-52C>A
ENST00000528996.1:c.451-52C>A	ENSP00000431226.1:n.451-52C>A
ENST00000530113.1:n.707-52C>A
ENST00000531133.5:c.751-52C>A	ENSP00000435431.1:n.751-52C>A
ENST00000531797.5:c.*275-52C>A	ENSP00000432554.1:n.*275-52C>A
ENST00000619430.1:c.381-52C>A	ENSP00000478572.1:n.381-52C>A
NM_000062.2:c.1250-52C>A , LRG_105t1:c.1250-52C>A	NP_000053.2:n.1250-52C>A
NM_001032295.1:c.1250-52C>A	NP_001027466.1:n.1250-52C>A
NM_000062.3:c.1250-52C>A MANE Select	NP_000053.2:n.1250-52C>A
NM_001032295.2:c.1250-52C>A	NP_001027466.1:n.1250-52C>A