Canonical Allele Identifier: CA397586685

Gene: SERPINF1

Linked Data

• MyVariant Identifiers: chr17:g.1675317G>T (hg19) ; chr17:g.1772023G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772023G>T , CM000679.2:g.1772023G>T	GRCh38
NC_000017.10:g.1675317G>T , CM000679.1:g.1675317G>T	GRCh37
NC_000017.9:g.1622067G>T	NCBI36
NG_028180.1:g.15059G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.591G>T MANE Select	ENSP00000254722.4:p.Lys197Asn
ENST00000254722.8:c.591G>T	ENSP00000254722.4:p.Lys197Asn
ENST00000570820.1:n.811G>T
ENST00000572048.1:c.30G>T	ENSP00000458484.1:p.Lys10Asn
ENST00000573763.1:c.-11G>T	ENSP00000461405.1:n.-11G>T
ENST00000576406.5:c.30G>T	ENSP00000461214.1:p.Lys10Asn
NM_002615.5:c.591G>T	NP_002606.3:p.Lys197Asn
NM_001329903.1:c.591G>T	NP_001316832.1:p.Lys197Asn
NM_001329904.1:c.30G>T	NP_001316833.1:p.Lys10Asn
NM_001329905.1:c.30G>T	NP_001316834.1:p.Lys10Asn
NM_002615.6:c.591G>T	NP_002606.3:p.Lys197Asn
NM_002615.7:c.591G>T MANE Select	NP_002606.3:p.Lys197Asn
NM_001329903.2:c.591G>T	NP_001316832.1:p.Lys197Asn
NM_001329904.2:c.30G>T	NP_001316833.1:p.Lys10Asn
NM_001329905.2:c.30G>T	NP_001316834.1:p.Lys10Asn