Canonical Allele Identifier: CA397587006

Gene: SERPINF1

Linked Data

• gnomAD v3: 17-1772069-T-A
• gnomAD v4: 17-1772069-T-A
• MyVariant Identifiers: chr17:g.1675363T>A (hg19) ; chr17:g.1772069T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772069T>A , CM000679.2:g.1772069T>A	GRCh38
NC_000017.10:g.1675363T>A , CM000679.1:g.1675363T>A	GRCh37
NC_000017.9:g.1622113T>A	NCBI36
NG_028180.1:g.15105T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.637T>A MANE Select	ENSP00000254722.4:p.Phe213Ile
ENST00000254722.8:c.637T>A	ENSP00000254722.4:p.Phe213Ile
ENST00000572048.1:c.76T>A	ENSP00000458484.1:p.Phe26Ile
ENST00000573763.1:c.36T>A	ENSP00000461405.1:p.Thr12=
ENST00000576406.5:c.76T>A	ENSP00000461214.1:p.Phe26Ile
NM_002615.5:c.637T>A	NP_002606.3:p.Phe213Ile
NM_001329903.1:c.637T>A	NP_001316832.1:p.Phe213Ile
NM_001329904.1:c.76T>A	NP_001316833.1:p.Phe26Ile
NM_001329905.1:c.76T>A	NP_001316834.1:p.Phe26Ile
NM_002615.6:c.637T>A	NP_002606.3:p.Phe213Ile
NM_002615.7:c.637T>A MANE Select	NP_002606.3:p.Phe213Ile
NM_001329903.2:c.637T>A	NP_001316832.1:p.Phe213Ile
NM_001329904.2:c.76T>A	NP_001316833.1:p.Phe26Ile
NM_001329905.2:c.76T>A	NP_001316834.1:p.Phe26Ile