Canonical Allele Identifier: CA397584305

Gene: SERPINF1

Linked Data

• ClinVar Variation Id: 2736388
• ClinVar RCV Id: RCV003559933
• MyVariant Identifiers: chr17:g.1673345G>T (hg19) ; chr17:g.1770051G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1770051G>T , CM000679.2:g.1770051G>T	GRCh38
NC_000017.10:g.1673345G>T , CM000679.1:g.1673345G>T	GRCh37
NC_000017.9:g.1620095G>T	NCBI36
NG_028180.1:g.13087G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.283+1G>T MANE Select	ENSP00000254722.4:n.283+1G>T
ENST00000254722.8:c.283+1G>T	ENSP00000254722.4:n.283+1G>T
ENST00000570731.5:c.283+1G>T	ENSP00000459869.1:n.283+1G>T
ENST00000571360.5:c.244+1G>T	ENSP00000461660.1:n.244+1G>T
ENST00000571870.5:n.524+1G>T
ENST00000573770.5:c.283+1G>T	ENSP00000459107.1:n.283+1G>T
ENST00000576406.5:c.-279+1G>T	ENSP00000461214.1:n.-279+1G>T
ENST00000577053.1:c.283+1G>T	ENSP00000460842.1:n.283+1G>T
NM_002615.5:c.283+1G>T	NP_002606.3:n.283+1G>T
NM_001329903.1:c.283+1G>T	NP_001316832.1:n.283+1G>T
NM_001329904.1:c.-279+1G>T	NP_001316833.1:n.-279+1G>T
NM_002615.6:c.283+1G>T	NP_002606.3:n.283+1G>T
NM_002615.7:c.283+1G>T MANE Select	NP_002606.3:n.283+1G>T
NM_001329903.2:c.283+1G>T	NP_001316832.1:n.283+1G>T
NM_001329904.2:c.-279+1G>T	NP_001316833.1:n.-279+1G>T