Canonical Allele Identifier: CA8274704

Gene: SERPINF1

Linked Data

• ClinVar Variation Id: 1635177
• ClinVar RCV Id: RCV002133253
• dbSNP Id: rs761557470
• ExAC: 17:1675149 G / C
• gnomAD v2: 17-1675149-G-C
• gnomAD v3: 17-1771855-G-C
• gnomAD v4: 17-1771855-G-C
• MyVariant Identifiers: chr17:g.1675149G>C (hg19) ; chr17:g.1771855G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1771855G>C , CM000679.2:g.1771855G>C	GRCh38
NC_000017.10:g.1675149G>C , CM000679.1:g.1675149G>C	GRCh37
NC_000017.9:g.1621899G>C	NCBI36
NG_028180.1:g.14891G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.440-17G>C MANE Select	ENSP00000254722.4:n.440-17G>C
ENST00000254722.8:c.440-17G>C	ENSP00000254722.4:n.440-17G>C
ENST00000570820.1:n.660-17G>C
ENST00000571870.5:n.681-17G>C
ENST00000572048.1:c.-139G>C	ENSP00000458484.1:n.-139G>C
ENST00000573763.1:c.-179G>C	ENSP00000461405.1:n.-179G>C
ENST00000573770.5:c.*290-17G>C	ENSP00000459107.1:n.*290-17G>C
ENST00000576406.5:c.-122-17G>C	ENSP00000461214.1:n.-122-17G>C
NM_002615.5:c.440-17G>C	NP_002606.3:n.440-17G>C
NM_001329903.1:c.440-17G>C	NP_001316832.1:n.440-17G>C
NM_001329904.1:c.-122-17G>C	NP_001316833.1:n.-122-17G>C
NM_001329905.1:c.-139G>C	NP_001316834.1:n.-139G>C
NM_002615.6:c.440-17G>C	NP_002606.3:n.440-17G>C
NM_002615.7:c.440-17G>C MANE Select	NP_002606.3:n.440-17G>C
NM_001329903.2:c.440-17G>C	NP_001316832.1:n.440-17G>C
NM_001329904.2:c.-122-17G>C	NP_001316833.1:n.-122-17G>C
NM_001329905.2:c.-139G>C	NP_001316834.1:n.-139G>C