Canonical Allele Identifier: CA397584179
Gene: SERPINF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1769982C>G , CM000679.2:g.1769982C>G GRCh38
NC_000017.10:g.1673276C>G , CM000679.1:g.1673276C>G GRCh37
NC_000017.9:g.1620026C>G NCBI36
NG_028180.1:g.13018C>G

Transcript Alleles

HGVS Amino-acid Change
NM_002615.7:c.215C>G MANE Select NP_002606.3:p.Thr72Arg
ENST00000254722.9:c.215C>G MANE Select ENSP00000254722.4:p.Thr72Arg
NM_001329903.1:c.215C>G NP_001316832.1:p.Thr72Arg
NM_001329903.2:c.215C>G NP_001316832.1:p.Thr72Arg
NM_001329904.1:c.-347C>G NP_001316833.1:n.-347C>G
NM_001329904.2:c.-347C>G NP_001316833.1:n.-347C>G
NM_002615.5:c.215C>G NP_002606.3:p.Thr72Arg
NM_002615.6:c.215C>G NP_002606.3:p.Thr72Arg
ENST00000254722.8:c.215C>G ENSP00000254722.4:p.Thr72Arg
ENST00000570731.5:c.215C>G ENSP00000459869.1:p.Thr72Arg
ENST00000571149.5:c.215C>G ENSP00000460905.1:p.Thr72Arg
ENST00000571360.5:c.176C>G ENSP00000461660.1:p.Thr59Arg
ENST00000571870.5:n.456C>G
ENST00000573770.5:c.215C>G ENSP00000459107.1:p.Thr72Arg
ENST00000576406.5:c.-347C>G ENSP00000461214.1:n.-347C>G
ENST00000577053.1:c.215C>G ENSP00000460842.1:p.Thr72Arg