Canonical Allele Identifier: CA380690350

Gene: SERPING1

Linked Data

• gnomAD v4: 11-57614375-G-A
• MyVariant Identifiers: chr11:g.57381848G>A (hg19) ; chr11:g.57614375G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.57614375G>A , CM000673.2:g.57614375G>A	GRCh38
NC_000011.9:g.57381848G>A , CM000673.1:g.57381848G>A	GRCh37
NC_000011.8:g.57138424G>A	NCBI36
NG_009625.1:g.21822G>A , LRG_105:g.21822G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000278407.9:c.1297G>A MANE Select	ENSP00000278407.4:p.Asp433Asn
ENST00000528996.2:c.*194G>A	ENSP00000431226.2:n.*194G>A
ENST00000531605.2:c.*1073G>A	ENSP00000503752.1:n.*1073G>A
ENST00000619430.2:c.1093G>A	ENSP00000478572.2:p.Asp365Asn
ENST00000676670.1:c.1297G>A	ENSP00000504807.1:p.Asp433Asn
ENST00000676741.1:n.2379G>A
ENST00000677624.1:c.*717G>A	ENSP00000503979.1:n.*717G>A
ENST00000677625.1:c.1243G>A	ENSP00000502857.1:p.Asp415Asn
ENST00000677856.1:n.1550G>A
ENST00000677915.1:c.*194G>A	ENSP00000503118.1:n.*194G>A
ENST00000678533.1:c.*851G>A	ENSP00000503873.1:n.*851G>A
ENST00000678592.1:c.*237G>A	ENSP00000504424.1:n.*237G>A
ENST00000278407.8:c.1297G>A	ENSP00000278407.4:p.Asp433Asn
ENST00000340687.10:c.1186G>A	ENSP00000341861.6:p.Asp396Asn
ENST00000378323.8:c.1312G>A	ENSP00000367574.4:p.Asp438Asn
ENST00000378324.6:c.1141G>A	ENSP00000367575.2:p.Asp381Asn
ENST00000403558.1:c.1426G>A	ENSP00000384420.1:p.Asp476Asn
ENST00000528996.1:c.498G>A	ENSP00000431226.1:n.498G>A
ENST00000530113.1:n.754G>A
ENST00000531133.5:c.798G>A	ENSP00000435431.1:n.798G>A
ENST00000531797.5:c.*322G>A	ENSP00000432554.1:n.*322G>A
ENST00000619430.1:c.428G>A	ENSP00000478572.1:n.428G>A
NM_000062.2:c.1297G>A , LRG_105t1:c.1297G>A	NP_000053.2:p.Asp433Asn
NM_001032295.1:c.1297G>A	NP_001027466.1:p.Asp433Asn
NM_000062.3:c.1297G>A MANE Select	NP_000053.2:p.Asp433Asn
NM_001032295.2:c.1297G>A	NP_001027466.1:p.Asp433Asn