Canonical Allele Identifier: CA397586838

Gene: SERPINF1

Linked Data

• MyVariant Identifiers: chr17:g.1675340T>C (hg19) ; chr17:g.1772046T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1772046T>C , CM000679.2:g.1772046T>C	GRCh38
NC_000017.10:g.1675340T>C , CM000679.1:g.1675340T>C	GRCh37
NC_000017.9:g.1622090T>C	NCBI36
NG_028180.1:g.15082T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000254722.9:c.614T>C MANE Select	ENSP00000254722.4:p.Ile205Thr
ENST00000254722.8:c.614T>C	ENSP00000254722.4:p.Ile205Thr
ENST00000572048.1:c.53T>C	ENSP00000458484.1:p.Ile18Thr
ENST00000573763.1:c.13T>C	ENSP00000461405.1:p.Phe5Leu
ENST00000576406.5:c.53T>C	ENSP00000461214.1:p.Ile18Thr
NM_002615.5:c.614T>C	NP_002606.3:p.Ile205Thr
NM_001329903.1:c.614T>C	NP_001316832.1:p.Ile205Thr
NM_001329904.1:c.53T>C	NP_001316833.1:p.Ile18Thr
NM_001329905.1:c.53T>C	NP_001316834.1:p.Ile18Thr
NM_002615.6:c.614T>C	NP_002606.3:p.Ile205Thr
NM_002615.7:c.614T>C MANE Select	NP_002606.3:p.Ile205Thr
NM_001329903.2:c.614T>C	NP_001316832.1:p.Ile205Thr
NM_001329904.2:c.53T>C	NP_001316833.1:p.Ile18Thr
NM_001329905.2:c.53T>C	NP_001316834.1:p.Ile18Thr