Canonical Allele Identifier: CA397586999

Gene: SERPINF1

Linked Data

• dbSNP Id: rs1907779001
• MyVariant Identifiers: chr17:g.1675362C>A (hg19) ; chr17:g.1772068C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772068C>A , CM000679.2:g.1772068C>A	GRCh38
NC_000017.10:g.1675362C>A , CM000679.1:g.1675362C>A	GRCh37
NC_000017.9:g.1622112C>A	NCBI36
NG_028180.1:g.15104C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.636C>A MANE Select	ENSP00000254722.4:p.His212Gln
ENST00000254722.8:c.636C>A	ENSP00000254722.4:p.His212Gln
ENST00000572048.1:c.75C>A	ENSP00000458484.1:p.His25Gln
ENST00000573763.1:c.35C>A	ENSP00000461405.1:p.Thr12Asn
ENST00000576406.5:c.75C>A	ENSP00000461214.1:p.His25Gln
NM_002615.5:c.636C>A	NP_002606.3:p.His212Gln
NM_001329903.1:c.636C>A	NP_001316832.1:p.His212Gln
NM_001329904.1:c.75C>A	NP_001316833.1:p.His25Gln
NM_001329905.1:c.75C>A	NP_001316834.1:p.His25Gln
NM_002615.6:c.636C>A	NP_002606.3:p.His212Gln
NM_002615.7:c.636C>A MANE Select	NP_002606.3:p.His212Gln
NM_001329903.2:c.636C>A	NP_001316832.1:p.His212Gln
NM_001329904.2:c.75C>A	NP_001316833.1:p.His25Gln
NM_001329905.2:c.75C>A	NP_001316834.1:p.His25Gln