Canonical Allele Identifier: CA397586718

Gene: SERPINF1

Linked Data

• MyVariant Identifiers: chr17:g.1675321A>T (hg19) ; chr17:g.1772027A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772027A>T , CM000679.2:g.1772027A>T	GRCh38
NC_000017.10:g.1675321A>T , CM000679.1:g.1675321A>T	GRCh37
NC_000017.9:g.1622071A>T	NCBI36
NG_028180.1:g.15063A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.595A>T MANE Select	ENSP00000254722.4:p.Ile199Phe
ENST00000254722.8:c.595A>T	ENSP00000254722.4:p.Ile199Phe
ENST00000570820.1:n.815A>T
ENST00000572048.1:c.34A>T	ENSP00000458484.1:p.Ile12Phe
ENST00000573763.1:c.-7A>T	ENSP00000461405.1:n.-7A>T
ENST00000576406.5:c.34A>T	ENSP00000461214.1:p.Ile12Phe
NM_002615.5:c.595A>T	NP_002606.3:p.Ile199Phe
NM_001329903.1:c.595A>T	NP_001316832.1:p.Ile199Phe
NM_001329904.1:c.34A>T	NP_001316833.1:p.Ile12Phe
NM_001329905.1:c.34A>T	NP_001316834.1:p.Ile12Phe
NM_002615.6:c.595A>T	NP_002606.3:p.Ile199Phe
NM_002615.7:c.595A>T MANE Select	NP_002606.3:p.Ile199Phe
NM_001329903.2:c.595A>T	NP_001316832.1:p.Ile199Phe
NM_001329904.2:c.34A>T	NP_001316833.1:p.Ile12Phe
NM_001329905.2:c.34A>T	NP_001316834.1:p.Ile12Phe