Canonical Allele Identifier: CA397586760

Gene: SERPINF1

Linked Data

• dbSNP Id: rs1907776686
• gnomAD v3: 17-1772035-T-A
• gnomAD v4: 17-1772035-T-A
• MyVariant Identifiers: chr17:g.1675329T>A (hg19) ; chr17:g.1772035T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772035T>A , CM000679.2:g.1772035T>A	GRCh38
NC_000017.10:g.1675329T>A , CM000679.1:g.1675329T>A	GRCh37
NC_000017.9:g.1622079T>A	NCBI36
NG_028180.1:g.15071T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.603T>A MANE Select	ENSP00000254722.4:p.Asp201Glu
ENST00000254722.8:c.603T>A	ENSP00000254722.4:p.Asp201Glu
ENST00000572048.1:c.42T>A	ENSP00000458484.1:p.Asp14Glu
ENST00000573763.1:c.2T>A	ENSP00000461405.1:p.Met1Lys
ENST00000576406.5:c.42T>A	ENSP00000461214.1:p.Asp14Glu
NM_002615.5:c.603T>A	NP_002606.3:p.Asp201Glu
NM_001329903.1:c.603T>A	NP_001316832.1:p.Asp201Glu
NM_001329904.1:c.42T>A	NP_001316833.1:p.Asp14Glu
NM_001329905.1:c.42T>A	NP_001316834.1:p.Asp14Glu
NM_002615.6:c.603T>A	NP_002606.3:p.Asp201Glu
NM_002615.7:c.603T>A MANE Select	NP_002606.3:p.Asp201Glu
NM_001329903.2:c.603T>A	NP_001316832.1:p.Asp201Glu
NM_001329904.2:c.42T>A	NP_001316833.1:p.Asp14Glu
NM_001329905.2:c.42T>A	NP_001316834.1:p.Asp14Glu