Canonical Allele Identifier: CA8274724

Gene: SERPINF1

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.1771941C>T , CM000679.2:g.1771941C>T	GRCh38
NC_000017.10:g.1675235C>T , CM000679.1:g.1675235C>T	GRCh37
NC_000017.9:g.1621985C>T	NCBI36
NG_028180.1:g.14977C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_002615.7:c.509C>T MANE Select	NP_002606.3:p.Thr170Met
ENST00000254722.9:c.509C>T MANE Select	ENSP00000254722.4:p.Thr170Met
NM_001329903.1:c.509C>T	NP_001316832.1:p.Thr170Met
NM_001329903.2:c.509C>T	NP_001316832.1:p.Thr170Met
NM_001329904.1:c.-53C>T	NP_001316833.1:n.-53C>T
NM_001329904.2:c.-53C>T	NP_001316833.1:n.-53C>T
NM_001329905.1:c.-53C>T	NP_001316834.1:n.-53C>T
NM_001329905.2:c.-53C>T	NP_001316834.1:n.-53C>T
NM_002615.5:c.509C>T	NP_002606.3:p.Thr170Met
NM_002615.6:c.509C>T	NP_002606.3:p.Thr170Met
ENST00000254722.8:c.509C>T	ENSP00000254722.4:p.Thr170Met
ENST00000570820.1:n.729C>T
ENST00000572048.1:c.-53C>T	ENSP00000458484.1:n.-53C>T
ENST00000573763.1:c.-93C>T	ENSP00000461405.1:n.-93C>T
ENST00000573770.5:c.*359C>T	ENSP00000459107.1:n.*359C>T
ENST00000576406.5:c.-53C>T	ENSP00000461214.1:n.-53C>T