Canonical Allele Identifier: CA397586868

Gene: SERPINF1

Linked Data

• MyVariant Identifiers: chr17:g.1675343T>A (hg19) ; chr17:g.1772049T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772049T>A , CM000679.2:g.1772049T>A	GRCh38
NC_000017.10:g.1675343T>A , CM000679.1:g.1675343T>A	GRCh37
NC_000017.9:g.1622093T>A	NCBI36
NG_028180.1:g.15085T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.617T>A MANE Select	ENSP00000254722.4:p.Leu206His
ENST00000254722.8:c.617T>A	ENSP00000254722.4:p.Leu206His
ENST00000572048.1:c.56T>A	ENSP00000458484.1:p.Leu19His
ENST00000573763.1:c.16T>A	ENSP00000461405.1:p.Ser6Thr
ENST00000576406.5:c.56T>A	ENSP00000461214.1:p.Leu19His
NM_002615.5:c.617T>A	NP_002606.3:p.Leu206His
NM_001329903.1:c.617T>A	NP_001316832.1:p.Leu206His
NM_001329904.1:c.56T>A	NP_001316833.1:p.Leu19His
NM_001329905.1:c.56T>A	NP_001316834.1:p.Leu19His
NM_002615.6:c.617T>A	NP_002606.3:p.Leu206His
NM_002615.7:c.617T>A MANE Select	NP_002606.3:p.Leu206His
NM_001329903.2:c.617T>A	NP_001316832.1:p.Leu206His
NM_001329904.2:c.56T>A	NP_001316833.1:p.Leu19His
NM_001329905.2:c.56T>A	NP_001316834.1:p.Leu19His