Canonical Allele Identifier: CA380695063

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57600123-C-A
• MyVariant Identifiers: chr11:g.57367596C>A (hg19) ; chr11:g.57600123C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57600123C>A , CM000673.2:g.57600123C>A	GRCh38
NC_000011.9:g.57367596C>A , CM000673.1:g.57367596C>A	GRCh37
NC_000011.8:g.57124172C>A	NCBI36
NG_009625.1:g.7570C>A , LRG_105:g.7570C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278407.9:c.296C>A MANE Select	ENSP00000278407.4:p.Thr99Asn
ENST00000528996.2:c.58+1795C>A	ENSP00000431226.2:n.58+1795C>A
ENST00000531605.2:c.51+1802C>A	ENSP00000503752.1:n.51+1802C>A
ENST00000619430.2:c.296C>A	ENSP00000478572.2:p.Thr99Asn
ENST00000676670.1:c.296C>A	ENSP00000504807.1:p.Thr99Asn
ENST00000676741.1:n.1378C>A
ENST00000677275.1:n.283C>A
ENST00000677624.1:c.296C>A	ENSP00000503979.1:p.Thr99Asn
ENST00000677625.1:c.296C>A	ENSP00000502857.1:p.Thr99Asn
ENST00000677856.1:n.355C>A
ENST00000677915.1:c.296C>A	ENSP00000503118.1:p.Thr99Asn
ENST00000678533.1:c.51+1802C>A	ENSP00000503873.1:n.51+1802C>A
ENST00000678592.1:c.296C>A	ENSP00000504424.1:p.Thr99Asn
ENST00000278407.8:c.296C>A	ENSP00000278407.4:p.Thr99Asn
ENST00000340687.10:c.296C>A	ENSP00000341861.6:p.Thr99Asn
ENST00000378323.8:c.311C>A	ENSP00000367574.4:p.Thr104Asn
ENST00000378324.6:c.140C>A	ENSP00000367575.2:p.Thr47Asn
ENST00000403558.1:c.398C>A	ENSP00000384420.1:p.Thr133Asn
ENST00000405496.5:c.296C>A	ENSP00000384561.1:p.Thr99Asn
ENST00000531133.5:c.51+1802C>A	ENSP00000435431.1:n.51+1802C>A
ENST00000531797.5:c.51+1802C>A	ENSP00000432554.1:n.51+1802C>A
ENST00000619430.1:c.296C>A	ENSP00000478572.1:p.Thr99Asn
NM_000062.2:c.296C>A , LRG_105t1:c.296C>A	NP_000053.2:p.Thr99Asn
NM_001032295.1:c.296C>A	NP_001027466.1:p.Thr99Asn
NM_000062.3:c.296C>A MANE Select	NP_000053.2:p.Thr99Asn
NM_001032295.2:c.296C>A	NP_001027466.1:p.Thr99Asn