Canonical Allele Identifier: CA8274517

Gene: SERPINF1

Linked Data

• ClinVar Variation Id: 1665650
• ClinVar RCV Id: RCV002193829
• dbSNP Id: rs775909358
• ExAC: 17:1670303 G / A
• gnomAD v2: 17-1670303-G-A
• gnomAD v3: 17-1767009-G-A
• gnomAD v4: 17-1767009-G-A
• MyVariant Identifiers: chr17:g.1670303G>A (hg19) ; chr17:g.1767009G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1767009G>A , CM000679.2:g.1767009G>A	GRCh38
NC_000017.10:g.1670303G>A , CM000679.1:g.1670303G>A	GRCh37
NC_000017.9:g.1617053G>A	NCBI36
NG_028180.1:g.10045G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.84+15G>A MANE Select	ENSP00000254722.4:n.84+15G>A
ENST00000254722.8:c.84+15G>A	ENSP00000254722.4:n.84+15G>A
ENST00000570731.5:c.84+15G>A	ENSP00000459869.1:n.84+15G>A
ENST00000571149.5:c.84+15G>A	ENSP00000460905.1:n.84+15G>A
ENST00000571360.5:c.84+15G>A	ENSP00000461660.1:n.84+15G>A
ENST00000571870.5:n.145+15G>A
ENST00000573770.5:c.84+15G>A	ENSP00000459107.1:n.84+15G>A
ENST00000576406.5:c.-477-2843G>A	ENSP00000461214.1:n.-477-2843G>A
ENST00000577053.1:c.84+15G>A	ENSP00000460842.1:n.84+15G>A
NM_002615.5:c.84+15G>A	NP_002606.3:n.84+15G>A
NM_001329903.1:c.84+15G>A	NP_001316832.1:n.84+15G>A
NM_001329904.1:c.-477-2843G>A	NP_001316833.1:n.-477-2843G>A
NM_002615.6:c.84+15G>A	NP_002606.3:n.84+15G>A
NM_002615.7:c.84+15G>A MANE Select	NP_002606.3:n.84+15G>A
NM_001329903.2:c.84+15G>A	NP_001316832.1:n.84+15G>A
NM_001329904.2:c.-477-2843G>A	NP_001316833.1:n.-477-2843G>A