Canonical Allele Identifier: CA286843732
Gene: SERPINF1 HGNC NCBI
dbSNP:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.1770111G>T , CM000679.2:g.1770111G>T GRCh38
NC_000017.10:g.1673405G>T , CM000679.1:g.1673405G>T GRCh37
NC_000017.9:g.1620155G>T NCBI36
NG_028180.1:g.13147G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000254722.9:c.283+61G>T MANE Select ENSP00000254722.4:n.283+61G>T
ENST00000254722.8:c.283+61G>T ENSP00000254722.4:n.283+61G>T
ENST00000570731.5:c.283+61G>T ENSP00000459869.1:n.283+61G>T
ENST00000571360.5:c.244+61G>T ENSP00000461660.1:n.244+61G>T
ENST00000571870.5:n.524+61G>T
ENST00000573770.5:c.283+61G>T ENSP00000459107.1:n.283+61G>T
ENST00000576406.5:c.-279+61G>T ENSP00000461214.1:n.-279+61G>T
ENST00000577053.1:c.283+61G>T ENSP00000460842.1:n.283+61G>T
NM_002615.5:c.283+61G>T NP_002606.3:n.283+61G>T
NM_001329903.1:c.283+61G>T NP_001316832.1:n.283+61G>T
NM_001329904.1:c.-279+61G>T NP_001316833.1:n.-279+61G>T
NM_002615.6:c.283+61G>T NP_002606.3:n.283+61G>T
NM_002615.7:c.283+61G>T MANE Select NP_002606.3:n.283+61G>T
NM_001329903.2:c.283+61G>T NP_001316832.1:n.283+61G>T
NM_001329904.2:c.-279+61G>T NP_001316833.1:n.-279+61G>T